Skip to content

Ace S2-71

by Alfa Wassermann, Inc.

Ace S2-71 is a Class II device made by Alfa Wassermann, Inc., listed in FDA GUDID since 24 Sep 2016 (UDI-DI 00857969006013), registry data as of 22 Oct 2026.

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

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00857969006013 UDI-DI Date24 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Ace
Generic name
Low density lipoprotein (LDL) cholesterol IVD, calibrator
Model / Ref / Catalog
S2-71
Primary DI / UDI-DI
00857969006013
FDA product code
JIS
GMDN term
Low density lipoprotein (LDL) cholesterol IVD, calibrator
Device class
Class II
Regulation number
862.1150
GUDID distribution status
In Commercial Distribution

Related devices

Category: Low density lipoprotein (LDL) cholesterol IVD, calibrator

Other devices from Alfa Wassermann, Inc.

See all devices from Alfa Wassermann, Inc. →

Properties

  • Convenience kit
  • Lot / batch number
  • Expiration date
Other properties (12, all answered No)