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Sth1

FDA UDI

Class I (US FDA UDI)

by American Diagnostic Corporation

Identity

Trade Name
STH1 FDA UDI
Generic Name
Mechanical external stethoscope FDA UDI
Device Name
STH1 Scope Tape Holder,Purple FDA UDI
Model / Reference
219V FDA UDI
Description
STH1 Scope Tape Holder,Purple FDA UDI

Identifiers

Catalog Number
219V FDA UDI
Primary DI / UDI-DI
00634782082864 FDA UDI
FDA Product Code
LDE FDA UDI
GMDN Term
Mechanical external stethoscope FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
870.1875 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Sth1 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 360f0c0b-36f3-4611-a1be-8ae95caced4d 35 fields · synced May 30, 2026