Convertors 9185

by Cardinal Health 200, LLC 3 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	Number10630140166150 UDI-DI	Date28 Jun 2016Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: Convertors
Generic Name: General surgical procedure kit, non-medicated, single-use
Model / Ref / Catalog: 9185

Primary DI / UDI-DI: 10630140166150
FDA Product Code: LRO
GMDN Term: General surgical procedure kit, non-medicated, single-use

Device Class: Class II
Regulation Number: 878.4370
GUDID distribution status: In Commercial Distribution

Other devices from Cardinal Health 200, LLC

See all devices from Cardinal Health 200, LLC →

Properties

Sterile
Single Use
Over-the-Counter
Convenience Kit
Premarket Exempt
Lot / Batch Number
Expiration Date

Other properties (7)

Implantable: No
Contains Latex: No
Prescription Use: No
Combination Product: No
HCT/P: No
Serial Number: No
Manufacturing Date: No