Littmann®

3M™ Littmann® Electronic Stethoscope, TeleSteth™ Teleauscultation, Gray, 27" 3200T

Registry build 21.09.26
3manufacturers in China registered for this device type
13catalogue numbers in this listing
6510(k) clearances naming this product code

Who Else Makes It

Concentrated in Zhejiang (1), Guangdong (1), Jiangsu (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code DQD
Manufacturer City Province Registered as Device types
Yahorng Dongguan Electronic Co Ltd Guangdong Guangdong Contract manufacturer 8
ADC Ningbo Co., Ltd. Ningbo Zhejiang Exporter 13
Suzhou Melodicare Medical Technology Co., Ltd. Suzhou Jiangsu Manufacturer 3

Record

Regulatory record for Littmann®
Listed by 3M Company, United States
FDA product code DQD
Device type Stethoscope, Electronic
Device class Class 2
Regulation 21 CFR 870.1875
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
510(k) K083903
Record published 2016-09-24
Record revised 2026-03-30 (version 7)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Latex Labelled latex-free
Label carries lot or batch number, manufacturing date
Packaging Box of 3

Catalogue Numbers

Catalogue numbers for Littmann®
Catalogue number Size Status
3100BU In distribution
3100NB In distribution
3100NB In distribution
3200BU In distribution
3100BK27 In distribution
3100BU In distribution
3200NB In distribution
3100BK27 In distribution
3200BU In distribution
3200BK27 In distribution
3200NB In distribution
3200T In distribution
3200BK27 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
3M™ Littmann® 3M Company 29
Adscope® American Diagnostic Corp. 14
RNK Products Rnk Products, Inc. 10
Tyto Stethoscope Tyto Care, Ltd. 5
Steth IO Steth IO 4
Heroic Faith Heroic Faith International Ltd. 3
Stethophone Pro Sparrow Acoustics Inc. 2
AeviceMD Aevice Health Pte. Ltd. 2
Eko Core 500 and CAC500 Founder’s Edition bundle Eko Devices, Inc. 1
Eko Core 500 and CAC500 Standard bundle Eko Devices, Inc. 1
Stethophone Sparrow Acoustics Inc. 1
Core 500 Digital Stethoscope – Bundle-ROG Eko Devices, Inc. 1

Showing 12 of 79. All products under Stethoscope, Electronic

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K083903 2009-07-15
K051790 2005-07-25
K050159 2005-02-22
K041934 2004-10-15
K003723 2001-03-27
K771653 1977-09-12

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer