Medline Industries, Inc. DYNSCS20100

by Medline Industries, 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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number10193489895407 UDI-DI	Date21 Jul 2024Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: Medline Industries, Inc.
Generic Name: General surgical procedure kit, non-medicated, single-use
Model / Ref / Catalog: DYNSCS20100

Primary DI / UDI-DI: 10193489895407
FDA Product Code: FOZ
GMDN Term: General surgical procedure kit, non-medicated, single-use

Device Class: Class II
Regulation Number: 880.5200
GUDID distribution status: In Commercial Distribution

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Properties

Sterile
Single Use
Prescription Use
Convenience Kit
Lot / Batch Number

Other properties (9)

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