2AR5N530

FCC ID

Equipment: Wearable EMS (Electrical Muscle Stimulation)

Bio-Medical Research Limited 530

Parkmore Business Park West, Galway, N/A H91 NHT7 Ireland

Application
Frequency Range
Final Action Date
Granted
lWD0sACLhHY6gbJoUHSEbw==
2402.0-2480.0
2019-10-09
APPROVED
File NameDocument TypeDateDirect
Test ReportTest Report 2019-10-09 00:00:00 pdf
RF Exposure EvaluationRF Exposure Info 2019-10-09 00:00:00 pdf
Label InfoID Label/Location Info 2019-10-09 00:00:00 pdf
ST Confidentiality LetterCover Letter(s) 2019-10-09 00:00:00 pdf
Confidentiality RequestCover Letter(s) 2019-10-09 00:00:00 pdf
Authorisation LetterCover Letter(s) 2019-10-09 00:00:00 pdf
Block DiagramBlock Diagram N/A
External PhotosExternal Photos 2020-04-06 00:00:00 N/A
Internal PhotosInternal Photos 2020-04-06 00:00:00 N/A
Operational Description 2Operational Description N/A
Operational Description 1Operational Description N/A
Tune Uo InfoParts List/Tune Up Info N/A
SchematicsSchematics N/A
Test Set UpTest Setup Photos 2020-04-06 00:00:00 N/A
User ManualUsers Manual 2020-04-06 00:00:00 N/A

Application Details:

EquipmentWearable EMS (Electrical Muscle Stimulation)
FRN0028088243
Grantee Code2AR5N
Product Code530
Applicant BusinessBio-Medical Research Limited
Business AddressParkmore Business Park West , Galway,N/A Ireland H91 NHT7
TCB ScopeA4: UNII devices & low power transmitters using spread spectrum techniques
TCB Email[email protected]
ApplicantAlan Staunton –
Applicant Phone
Applicant Fax+353 (0)91 774301
Applicant Email[email protected]
Applicant MailStop
Test FirmUL VS Ltd
Test Firm ContactDavid Chawira
Test Firm Phone
Test Firm Fax00-44-1256-312001
Test Firm Email[email protected]
Certified ByM Kilkelly – Quality Manager
Comment [lWD0sACLhHY6gbJoUHSEbw==]: Power is conducted. This equipment complies with FCC RF portable radiation exposure limits set forth for an uncontrolled environment. This device must not be co-located or operating in conjunction with any other antenna or transmitter except in accordance with FCC multi-transmitter product procedures. End-users must be provided with specific operating instructions for satisfying RF exposure compliance

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