Tablet Battery

FDA UDI

Class I (US FDA UDI)

by Orthosoft Inc

Identity

Trade Name: Tablet Battery FDA UDI
Generic Name: Noninvasive device battery charger FDA UDI
Model / Reference: 20-8060-402-00 FDA UDI

Identifiers

Catalog Number: 20-8060-402-00 FDA UDI
Primary DI / UDI-DI: 00887868523908 FDA UDI
510(k) Number: K210998 FDA UDI
FDA Product Code: MOQ FDA UDI
GMDN Term: Noninvasive device battery charger 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

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Noninvasive device battery charger

Tablet Battery by Orthosoft Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

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: Orthosoft Inc

Sources (1)

FDA UDI 213ac3df-ab2c-4f7f-8154-82bc49f68a3d 35 fields · synced Jun 1, 2026