Ochsner-Kocher artery forceps 40-650-39

by Spiggle & Theis Medizintechnik GmbH

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	Number04250676744753 UDI-DI	Date30 Jul 2025Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: Ochsner-Kocher artery forceps
Generic Name: Surgical soft-tissue manipulation forceps, alligator, reusable
Model / Ref / Catalog: 40-650-39
Description: straight, 1:2 teeth 20 cm

Primary DI / UDI-DI: 04250676744753
FDA Product Code: KAE
GMDN Term: Surgical soft-tissue manipulation forceps, alligator, reusable

Device Class: Class I
Regulation Number: 874.4420
GUDID distribution status: In Commercial Distribution

Sterilization Method: Moist Heat or Steam Sterilization

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Properties

Prescription Use
Premarket Exempt
Lot / Batch Number
Manufacturing Date

Other properties (10)

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