Membrane Holding Forceps Ring 13-0127

by W.H. Holden, Inc.

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	NumberD9281301270 UDI-DI	Date19 Dec 2023Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: Membrane Holding Forceps Ring
Generic Name: Surgical soft-tissue manipulation forceps, tweezers-like, reusable
Model / Reference: 13-0127

Primary DI / UDI-DI: D9281301270
FDA Product Code: HTC
GMDN Term: Surgical soft-tissue manipulation forceps, tweezers-like, 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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See all devices from W.H. Holden, Inc. →

Properties

Premarket Exempt
Lot / Batch Number
Manufacturing Date

Other properties (11)

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
Serial Number: No
Expiration Date: No