JOSEPH LAMELAS Atrial Lift System MI-ALS-001

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	Number08022057015747 UDI-DI	Date3 Feb 2026Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: JOSEPH LAMELAS Atrial Lift System
Generic Name: Atrial retractor
Model / Ref / Catalog: MI-ALS-001

Primary DI / UDI-DI: 08022057015747
FDA Product Code: DWS
GMDN Term: Atrial retractor

Device Class: Class I
Regulation Number: 870.4500
GUDID distribution status: In Commercial Distribution

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Properties

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

Other properties (8)

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