Adc®

FDA UDI

Class I (US FDA UDI)

by American Diagnostic Corporation

Identity

Trade Name: ADC® FDA UDI
Generic Name: Manual goniometer FDA UDI
Device Name: PT Kit, FDA UDI
Model / Reference: 39800 FDA UDI
Description: PT Kit, FDA UDI

Identifiers

Catalog Number: 39800 FDA UDI
Primary DI / UDI-DI: 00634782099060 FDA UDI
FDA Product Code: KQW FDA UDI
GWZ FDA UDI
GMDN Term: Manual goniometer FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 888.1520 FDA UDI
882.1700 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Percussion hammer, manual, reusable Manual goniometer

Adc® by American Diagnostic Corporation — 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: American Diagnostic Corporation

Sources (1)

FDA UDI d9b917de-e9fe-4a9f-a0db-822b492cfbce 35 fields · synced Jun 1, 2026