Interstate All Battery

FDA UDI

Class I (US FDA UDI)

by Interstate All Battery Center

Identity

Trade Name: Interstate All Battery FDA UDI
Generic Name: Portable/mobile rechargeable battery pack FDA UDI
Device Name: 6V 5AH NICD PLUG FDA UDI
Model / Reference: MED2015 FDA UDI
Description: 6V 5AH NICD PLUG FDA UDI

Identifiers

Primary DI / UDI-DI: 00656489211200 FDA UDI
FDA Product Code: MOQ FDA UDI
GMDN Term: Portable/mobile rechargeable battery pack FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4820 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Portable/mobile rechargeable battery pack

Interstate All Battery by Interstate All Battery Center — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Interstate All Battery Center

Sources (1)

FDA UDI 1cd088c2-9946-4ec8-a45a-807eb731cad9 33 fields · synced May 30, 2026