Codman® 802913

by Integra LifeSciences Production Corporation

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	Number10381780516354 UDI-DI	Date28 Feb 2020Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 10381780516354

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Codman®
Generic name: Open-surgery electrosurgical handpiece/electrode, bipolar, reusable
Model / Ref / Catalog: 802913, 80-2913

Primary DI / UDI-DI: 10381780516354
FDA product code: GEI
GMDN term: Open-surgery electrosurgical handpiece/electrode, bipolar, reusable

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

Sterilisation method: Moist Heat or Steam Sterilization

Size: Length — 5 Inch
Length — 13 Centimeter

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Properties

Sterilise before use
Prescription use
Lot / batch number
Manufacturing date

Other properties (11)

Supplied 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