Tissue Liberator Blade Up

by T.A.G Medical Products Agricultural Cooperative Association 4 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 19 Oct 2026. What this means

Regulatory status

as of registry sync 19 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number10810190018191 UDI-DI	Date24 Sep 2016Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Generic Name: Bone file/rasp, manual, reusable
Model / Ref / Catalog: B, 902100t

Primary DI / UDI-DI: 10810190018191
FDA Product Code: LXH
GMDN Term: Bone file/rasp, manual, reusable

Device Class: Class I
Regulation Number: 888.4540
GUDID distribution status: In Commercial Distribution

Sterilization Method: Moist Heat or Steam Sterilization

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Properties

Premarket Exempt
Lot / Batch Number
Serial Number
Manufacturing Date

Other properties (10)

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