Stethoscope duplex®, slate grey, aluminium, 4001-02

by Rudolf Riester GmbH & Co. KG

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number04045396118492 UDI-DI	Date28 Jan 2021Listed	StatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: Stethoscope duplex®, slate grey, aluminium,
Generic Name: Mechanical external stethoscope
Model / Ref / Catalog: 4001-02

Primary DI / UDI-DI: 04045396118492
510(k) Number: K944337
FDA Product Code: LDE
GMDN Term: Mechanical external stethoscope

Device Class: Class I
Regulation Number: 870.1875
GUDID distribution status: In Commercial Distribution

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Properties

Lot / Batch Number
Manufacturing Date

Other properties (12)

Sterile: No
Single Use: No
Implantable: No
Contains Latex: No
Prescription Use: No
Over-the-Counter: No
Convenience Kit: No
Combination Product: No
HCT/P: No
Premarket Exempt: No
Serial Number: No
Expiration Date: No