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Battery System

FDA UDI

Class I (US FDA UDI)

by Hugh Steeper Limited

Identity

Trade Name
BATTERY SYSTEM FDA UDI
Generic Name
Myoelectric hand prosthesis FDA UDI
Model / Reference
50MM KINISI SH WR HOUSING M12 FDA UDI

Identifiers

Catalog Number
BBSW50-M12 FDA UDI
Primary DI / UDI-DI
05063368529519 FDA UDI
FDA Product Code
IQZ FDA UDI
GMDN Term
Myoelectric hand prosthesis FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3420 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Myoelectric hand prosthesis

Battery System by Hugh Steeper Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Myoelectric hand prosthesis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hugh Steeper Limited

Sources (1)

  • FDA UDI 429aef22-0440-4928-a498-9e0623011f30 33 fields · synced Jun 6, 2026