Ambler Surgical Dolphin nose dissecting forceps

by Ambler Surgical, LLC 3 variants

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	Number00190660050986 UDI-DI	Date4 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Withdrawn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: Ambler Surgical
Generic Name: Rigid endoscopic tissue manipulation forceps, reusable
Model / Ref / Catalog: Dolphin nose dissecting forceps, 97-180

Primary DI / UDI-DI: 00190660050986
510(k) Number: K040855
FDA Product Code: GEI
GMDN Term: Rigid endoscopic tissue manipulation forceps, reusable

Device Class: Class II
Regulation Number: 878.4400
GUDID distribution status: In Commercial Distribution

Sterilization Method: Moist Heat or Steam Sterilization

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Properties

Prescription Use
Lot / Batch Number

Other properties (12)

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