N/A A-100-595

by Doppkon GmbH & Co. KG 2 variants

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

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	Number04262494461637 UDI-DI	Date8 Sep 2025Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Generic Name: Rigid endoscopic biopsy forceps, reusable
Model / Ref / Catalog: A-100-595
Description: Cup Forceps Straight Jaw D 2.0mm, WL 150mm

Primary DI / UDI-DI: 04262494461637
FDA Product Code: GEN
GMDN Term: Rigid endoscopic biopsy forceps, reusable

Device Class: Class I
Regulation Number: 878.4800
GUDID distribution status: In Commercial Distribution

Sterilization Method: Moist Heat or Steam Sterilization

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Class I
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N/A A-001-454

Class I
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Class I

See all devices from Doppkon GmbH & Co. KG →

Properties

Prescription Use
Premarket Exempt
Lot / Batch Number

Other properties (11)

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