PecaPusher(1061)

by Eca Medical Instruments

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	Number00850078396433 UDI-DI	Date29 Sep 2026Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Generic Name: Orthopaedic surgical procedure kit, non-medicated, single-use
Model / Ref / Catalog: 1061

Primary DI / UDI-DI: 00850078396433
FDA Product Code: LXH
GMDN Term: Orthopaedic surgical procedure kit, non-medicated, single-use

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

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Properties

Sterile
Single Use
Prescription Use
Convenience Kit
Premarket Exempt
Lot / Batch Number
Expiration Date
Manufacturing Date

Other properties (6)

Implantable: No
Contains Latex: No
Over-the-Counter: No
Combination Product: No
HCT/P: No
Serial Number: No