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Baum

FDA UDI

Class I (US FDA UDI)

by W.a. Baum Co., Inc.

Identity

Trade Name
BAUM FDA UDI
Generic Name
Mechanical external stethoscope FDA UDI
Device Name
Sprague Rappaport Style Mechanical Stethoscope With Black Non-Latex Tubing FDA UDI
Model / Reference
2700 FDA UDI
Description
Sprague Rappaport Style Mechanical Stethoscope With Black Non-Latex Tubing FDA UDI

Identifiers

Catalog Number
2700 FDA UDI
Primary DI / UDI-DI
00810010923653 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

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Mechanical external stethoscope

Baum by W.a. Baum Co., Inc. — 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

Manufacturer
W.a. Baum Co., Inc.

Sources (1)

  • FDA UDI e0d8049f-79f4-48c9-93b4-3aeff9908d32 35 fields · synced Jun 1, 2026