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Adscope®

FDA UDI

Class I (US FDA UDI)

by American Diagnostic Corporation

Identity

Trade Name
Adscope® FDA UDI
Generic Name
Mechanical external stethoscope FDA UDI
Device Name
Chestpiece-603,Adult, Black FDA UDI
Model / Reference
603-01BK FDA UDI
Description
Chestpiece-603,Adult, Black FDA UDI

Identifiers

Catalog Number
603-01BK FDA UDI
Primary DI / UDI-DI
00634782003449 FDA UDI
FDA Product Code
BZS FDA UDI
GMDN Term
Mechanical external stethoscope FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.1930 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

No

FDA UDI

Over-the-Counter

Yes

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: Mechanical external stethoscope

Adscope® by American Diagnostic Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Mechanical external stethoscope.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a2e3a7f5-b728-4f95-902f-6c6774889655 35 fields · synced May 31, 2026