Federal Communications Commission
Washington, D.C. 20554
May 9, 2012
Small Entity Compliance Guide
Medical Micro-Power Networks
Report and Order
WT Docket No. 09-36; RM-11404
Released: November 30, 2011
This Guide is prepared in accordance with the requirements of Section 212 of
the Small Business Regulatory Enforcement Fairness Act of 1996. It is intended
to help small entities—small businesses, small organizations (non-profits), and
small governmental jurisdictions—comply with the new rules adopted in the
above-referenced FCC rulemaking docket(s). This Guide is not intended to
replace the rules and, therefore, final authority rests solely with the rules.
Although we have attempted to cover all parts of the rules that might be
especially important to small entities, the coverage may not be exhaustive. This
Guide may, perhaps, not apply in a particular situation based upon the
circumstances, and the FCC retains the discretion to adopt approaches on a
case-by-case basis that may differ from this Guide, where appropriate. Any
decisions regarding a particular small entity will be based on the statute and
In any civil or administrative action against a small entity for a violation of
rules, the content of the Small Entity Compliance Guide may be considered as
evidence of the reasonableness or appropriateness of proposed fines, penalties or
damages. Interested parties are free to file comments regarding this Guide and
the appropriateness of its application to a particular situation; the FCC will
consider whether the recommendations or interpretations in the Guide are
appropriate in that situation. The FCC may decide to revise this Guide without
public notice to reflect changes in the FCC’s approach to implementing a rule,
or to clarify or update the text of the Guide. Direct your comments and
recommendations, or calls for further assistance, to the FCC’s Consumer
TTY: 1-888-TELL-FCC (1-888-835-5322)
Medical Micro-Power Networks
1. Objectives of the Proceeding
In the Report and Order
adopted November 30, 2011 in ET Docket 09-36, the Commission amended the
Part 95 rules governing MedRadio devices to enable networks of implanted medical devices called
medical micropower networks. Medical micro-power networks, or MMNs for short, are networks of
devices implanted within the human body that communicate with a programmer/controller device outside
the body using a wireless communication link. MMNs are used for the purpose of providing functional
electric stimulation, a technique using electric currents to activate and monitor nerves and muscles.
The existing MedRadio rules under Part 95 of the Commission’s rules allow implanted and body-worn
medical devices to operate in the 401-406 MHz band. The Report and Order
amends the MedRadio rules
to allow MMNs to operate in the 413-419 MHz, 426-432 MHz, 438-444 MHz, and 451-457 MHz
frequency bands on a secondary basis. These frequency bands are used for other purposes on a primary
basis such as Federal government and private land mobile radios, Federal government radars, and remote
broadcast of radio stations. Because MMNs will operate on a secondary basis, they may not cause
interference to and must accept interference from primary users of these frequency bands. Use of these
four frequency bands for medical devices is limited only to MMNs. Other medical devices such as
pacemakers, insulin pumps, hearing aids, and medical telemetry devices may not use these four frequency
A copy of this Report and Order
is available at: http://hraunfoss.fcc.gov/edocs_public/attachmatch/FCC-11-176A1.pdf
MMNs are defined in the Part 95 rules as follows:
An ultra-low power wideband network consisting of a MedRadio programmer/control
transmitter and medical implant transmitters, all of which transmit or receive non-
voice data or related device control commands for the purpose of facilitating
functional electric stimulation, a technique using electric currents to activate and
monitor nerves and muscles.
3. Restrictions on MMN Operation
Use of MMNs must comply with the following restrictions:
MMNs can only be used to provide functional electric stimulation.
MMNS can be used only for diagnostic and therapeutic purposes.
MMNs must be provided to a patient only under the direction of a duly authorized health care
MMNs may not cause harmful interference to other authorized stations operating in the 413-419
MHz, 426-432 MHz, 438-444 MHz, and 451-457 MHz bands.
MMNs must accept interference from other authorized stations operating in the 413-419 MHz,
426-432 MHz, 438-444 MHz, and 451-457 MHz bands.
MMN devices may not be used to relay information to other devices that are not part of the MMN
using the 413-419 MHz, 426-432 MHz, 438-444 MHz, and 451-457 MHz frequency bands.
An MMN programmer/controller may communicate with a programmer/controller of another
MMN to coordinate sharing of the wireless link.
Implanted MMN devices may only communicate with the programmer/controller for their MMN.
An MMN implanted device may not communicate directly with another MMN implanted device.
An MMN programmer/controller can only control implanted devices within one patient.
Multiple MMNs may be present within a patient.
MMN transmitters must be certificated by the FCC or a Telecommunications Certification Body
(TCB) designated by the FCC. To obtain certification the manufacturer must submit a
certification application accompanied by a measurement report showing compliance with the
FCC technical requirements to the Commission or TCB. See 47 C.F.R. § 2.1033 for the
certification application requirements or http://www.fcc.gov/encyclopedia/equipment
authorization-procedures for more information.
MMN devices are licensed by rule and as such, individual licenses are not required for MMN use.
4. Technical Requirements
MMNs must comply with a number of technical requirements designed to allow them to share the 413-
419 MHz, 426-432 MHz, 438-444 MHz, and 451-457 MHz frequency bands with primary users and other
MMNs. Basically, these requirements require the MMNs to be frequency agile so that they can switch
among the four frequency bands so as to continue operating when use of a particular frequency band
becomes too heavy. The requirements also limit the power and length of time that MMNs may transmit.
Specifically, these requirements are that:
Each MMN programmer/controller and implanted device must be capable of operating in any of
the 413-419 MHz, 426-432 MHz, 438-444 MHz, and 451-457 MHz frequency bands.
The programmer/controller and implanted devices that are part of a single MMN must operate in
the same frequency band.
MMN programmer/controllers must have the ability to operate in the presence of other primary
and secondary users in the 413-419 MHz, 426-432 MHz, 438-444 MHz, and 451-457 MHz
An MMN programmer/controller must be capable of monitoring the frequency band in which it is
operating at least once every second.
An MMN programmer/controller must be capable of monitoring alternate frequency bands (i.e.
the frequency bands on which it is not operating) within two seconds prior to executing a change
to an alternate frequency band.
If the MMN programmer/controller detects a signal lasting more than 50 milliseconds that has a
power greater than -60 dBm as received by a 0 dBi antenna in any 12.5 kHz bandwidth within the
authorized bandwidth of the MMN signal, the programmer/controller will move to another
frequency band within one second.
MMN transmitters are allowed a maximum emission bandwidth of six megahertz.
MMN transmitters shall transmit with a peak EIRP of the lesser of 1 mW or (10 log B – 7.782)
dBm, where B is the 20 dB emission bandwidth of the transmitted signal in megahertz. The peak
power spectral density of the transmitted signal shall not exceed 800 microwatts per megahertz in
any 1 megahertz band.
In the first 2.5 megahertz beyond any of the frequency bands authorized for MMN operation, the
EIRP level associated with any unwanted emission must be attenuated within a 1 megahertz
bandwidth by at least 20 dB relative to the maximum EIRP level within any 1 megahertz of the
fundamental emission. In addition, emissions from an MMN transmitter that are more than 2.5
megahertz beyond any of the frequency bands authorized for MMN operation must be less than
field strength limits specified in the Part 95 rules.
MMN programmer/controllers shall not transmit more than three percent of the time.
5. Labeling and Other Requirements
MMNs must comply with a number of other requirements designed to inform medical professionals about
the secondary status of MMNs and allow the Commission to enforce the Part 95 rules governing MMN
All non-implanted MMN devices must be made available for inspection upon request by an
authorized FCC representative.
Persons operating implanted MMN transmitters are required to cooperate reasonably with duly
authorized FCC representatives in the resolution of interference.
A disclosure statement as specified in the Part 95 rules must be included with each MMN
transmitting device. This disclosure statement warns that the device must accept interference
from and not cause interference to primary users sharing the same frequency bands. The
statement also warns that there is no guarantee that the MMN device will not receive interference.
The MMN programmer/control transmitters must be labeled with a statement as specified in the
Part 95 rules. The statement warns that the device may not cause interference to and must accept
interference from devices that are operating on a primary basis in the same frequency bands as the
MMN programmer/control transmitter.
MMN implant transmitters must be identified by a serial number that is assigned by the device
manufacturer. This serial number may be placed either on the device or in the instruction manual
for the transmitter.
6. Weblink and Citations
The Report and Order
adopted November 30, 2011: Amendment of Parts 2 and 95 of the Commission’s
Rules to Provide Additional Spectrum for the Medical Device Radiocommunication Service in the 413-
457 MHz band, ET Docket No. 09-36, RM-11404, FCC 11-176 (Released Nov. 30, 2011). Available at:
The Notice of Proposed Rulemaking
that preceded the November 30, 2011 Report and Order
Amendment of Parts 2 and 95 of the Commission's Rules to Provide Additional Spectrum for the Medical
Device Radiocommunication Service in the 413-457 MHz band, ET Docket No. 09-36, RM-11404, Notice of Proposed Rulemaking
, 24 FCC Rcd 3445 (2009). Available at: http://hraunfoss.fcc.gov/edocs_public/attachmatch/FCC-09-20A1.pdf
The Notice of Inquiry
regarding medical devices which proceeded the Notice of Proposed Rulemaking
Investigation of the Spectrum Requirements for Advanced Medical Technologies, ET Docket Nos. 06-
135, 05-213, 03-92, Notice of Proposed Rulemaking, Notice of Inquiry, and Order
, 21 FCC Rcd 8164
(2006). Available at: http://hraunfoss.fcc.gov/edocs_public/attachmatch/FCC-06-103A1.pdf
A Memorandum Opinion and Order
amending the Part 95 MedRadio rules: Investigation of the
Spectrum Requirements for Advanced Medical Technologies, ET Docket Nos. 06-135, 05-213, and 03-
92, Memorandum Opinion and Order,
25 FCC Rcd 10414 (2010). Available at: http://hraunfoss.fcc.gov/edocs_public/attachmatch/FCC-10-128A1.pdf
A previous small business compliance guide addressing the previous amendment to the MedRadio rules is
available at: http://hraunfoss.fcc.gov/edocs_public/attachmatch/DA-11-912A1.doc
The Report and Order
which adopted the Part 95 MedRadio rules that were amended by the November
30, 2011 Report and Order
: Investigation of the Spectrum Requirements for Advanced Medical
Technologies, ET Docket Nos. 06-135, 05-213, and 03-92, Report and Order,
24 FCC Rcd 3474 (2009).
Available at http://hraunfoss.fcc.gov/edocs_public/attachmatch/FCC-09-23A1.pdf
A previous small business compliance guide addressing the original MedRadio rules is available at: http://hraunfoss.fcc.gov/edocs_public/attachmatch/DA-10-815A1.pdf