FDA UDI In Commercial Distribution 🇺🇸 United States

emPOWER

DI: B155EM20 · Model: em2 · BIONX MEDICAL TECHNOLOGIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
emPOWER
Primary DI
B155EM20
Version / Model
em2
Company Name
BIONX MEDICAL TECHNOLOGIES, INC.
Labeler DUNS
788290471
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-27
Public Version
4
Public Version Date
2023-05-03
Public Version Status
Update
Public Device Record Key
ac6ecbb0-7b6f-4075-83ec-1e724dc69f3e

Device Description

emPOWER Battery

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
ISW Assembly, Knee/Shank/Ankle/Foot, External

GMDN Terms

Code Name
36534 Portable/mobile rechargeable battery pack

Identifiers

Type ID
Primary B155EM20