Meduloc Intramedullary Fracture Fixation (IFF) System 90-IFF-400900

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	Number00810184540427 UDI-DI	Date14 Jan 2026Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: Meduloc Intramedullary Fracture Fixation (IFF) System
Generic Name: General internal orthopaedic fixation system implantation kit
Model / Ref / Catalog: 90-IFF-400900

Primary DI / UDI-DI: 00810184540427
FDA Product Code: FSM
GMDN Term: General internal orthopaedic fixation system implantation kit

Device Class: Class I
Regulation Number: 878.4800
GUDID distribution status: In Commercial Distribution

Sterilization Method: Moist Heat or Steam Sterilization
MRI Safety: MR Unsafe

Other devices from Meduloc

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Properties

Premarket Exempt
Lot / Batch Number
Serial Number

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
Expiration Date: No
Manufacturing Date: No