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Unipower

FDA UDI

Class II (US FDA UDI)

by Unipower Corp.

Identity

Trade Name
Unipower FDA UDI
Generic Name
Portable/mobile rechargeable battery pack FDA UDI
Model / Reference
B11767 FDA UDI

Identifiers

Primary DI / UDI-DI
00817392020444 FDA UDI
510(k) Number
K940842 FDA UDI
FDA Product Code
LDD FDA UDI
GMDN Term
Portable/mobile rechargeable battery pack FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.5300 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Portable/mobile rechargeable battery pack

Unipower by Unipower Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Portable/mobile rechargeable battery pack.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Unipower Corp.

Sources (1)

  • FDA UDI 195fa4df-c077-449f-af8c-e580faae5bff 33 fields · synced May 30, 2026