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Littmann®

FDA UDI

Class II (US FDA UDI)

by 3m Company

Identity

Trade Name
Littmann® FDA UDI
Generic Name
Electronic acoustic stethoscope FDA UDI
Device Name
3M™ Littmann® Electronic Stethoscope, TeleSteth™ Teleauscultation, Gray, 27" 3200T FDA UDI
Model / Reference
3200T FDA UDI
Description
3M™ Littmann® Electronic Stethoscope, TeleSteth™ Teleauscultation, Gray, 27" 3200T FDA UDI

Identifiers

Catalog Number
3200T FDA UDI
Primary DI / UDI-DI
00707387770419 FDA UDI
510(k) Number
K083903 FDA UDI
FDA Product Code
DQD FDA UDI
GMDN Term
Electronic acoustic stethoscope FDA UDI

Classification

Device Class
Class II 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

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Electronic acoustic stethoscope

Littmann® by 3m Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electronic acoustic stethoscope.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
3m Company

Sources (1)

  • FDA UDI c6980307-f3b0-4eb1-ba4f-93a523a8af4d 36 fields · synced May 30, 2026