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3M™ Littmann®

FDA UDI

Class I (US FDA UDI)

by 3m Company

Identity

Trade Name
3M™ Littmann® FDA UDI
Generic Name
Mechanical external stethoscope FDA UDI
Device Name
3M™ Littmann® Cardiology IV™ Diagnostic Stethoscope, 6232, Smoke-finish Chestpiece, Black Tube FDA UDI
Model / Reference
6232 FDA UDI
Description
3M™ Littmann® Cardiology IV™ Diagnostic Stethoscope, 6232, Smoke-finish Chestpiece, Black Tube FDA UDI

Identifiers

Catalog Number
6232 FDA UDI
Primary DI / UDI-DI
00707387812003 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

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

Yes

FDA UDI

Category: Mechanical external stethoscope

3M™ Littmann® by 3m Company — 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
3m Company

Sources (1)

  • FDA UDI be6f0679-6403-40a0-9d96-e1f55557c961 35 fields · synced Jun 6, 2026