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Battery

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
Battery FDA UDI
Generic Name
Portable/mobile rechargeable battery pack FDA UDI
Device Name
Battery Only for #100-5500 FDA UDI
Model / Reference
100-5502 FDA UDI
Description
Battery Only for #100-5500 FDA UDI

Identifiers

Catalog Number
100-5502 FDA UDI
Primary DI / UDI-DI
00192896112124 FDA UDI
FDA Product Code
HPP FDA UDI
GMDN Term
Portable/mobile rechargeable battery pack FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4335 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

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Portable/mobile rechargeable battery pack

Battery by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Portable/mobile rechargeable battery pack.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b1f5e468-d073-436d-8d94-2cf44f4570de 35 fields · synced May 30, 2026