ACE Liquid 1767001
ACE Liquid 1767001 is a Class II device made by Sentinel Ch. Srl, listed in FDA GUDID since 29 Jul 2016 (UDI-DI 08058056681751), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number08058056681751 | Date29 Jul 2016 | StatusListed |
Official records
- AccessGUDID record 08058056681751
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- ACE Liquid
- Generic name
- Angiotensin converting enzyme (ACE) IVD, reagent
- Model / Ref / Catalog
- 1767001
- Primary DI / UDI-DI
- 08058056681751
- FDA product code
- KQN
- GMDN term
- Angiotensin converting enzyme (ACE) IVD, reagent
- Device class
- Class II
- Regulation number
- 862.1090
- GUDID distribution status
- In Commercial Distribution
- Size
- Total Volume — 40 Milliliter
Similar devices
Other devices filed under FDA product code KQN (Radioassay, Angiotensin Converting Enzyme).
- ANGIOTENSIN CONVERTING ENZYME ASSAY SYS by Ventrex Laboratories, Inc.
- ACE COLOR TEST by Hana Biologics, Inc.
- ALDOSTERONE DIRECT RIA KIT by Biotecx Laboratories, Inc.
- THERMO ELECTRON ANGIOTENSIN CONVERTING ENZYME INFINITY (ACE) REAGENT by Thermo-Electron Corp.
- BUEHLMANN LAB AS, ACE ANGIO CONV ENZYME KIN ASSAY by American Laboratory Products Company
- SIGMA ANGIOTENSIN CONVERTING ENZYME 305-UV by Sigma Diagnostics, Inc.
- ANGIOTENSIN CONVERTING ENZYME REA by American Laboratory Products Company
- ACE ACTIVITY MICROVIAL TEST SET by Ventrex Laboratories, Inc.