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ACE Liquid

FDA UDI

Class II (US FDA UDI)

by Sentinel Ch. Srl

Identity

Trade Name
ACE Liquid FDA UDI
Generic Name
Angiotensin converting enzyme (ACE) IVD, reagent FDA UDI
Device Name
ACE Liquid reagent is for use in the determination of Angiotensin converting enzyme (ACE) activity in human serum or plasma. For In Vitro Diagnostic use. FDA UDI
Model / Reference
1767001 FDA UDI
Description
ACE Liquid reagent is for use in the determination of Angiotensin converting enzyme (ACE) activity in human serum or plasma. For In Vitro Diagnostic use. FDA UDI

Identifiers

Catalog Number
1767001 FDA UDI
Primary DI / UDI-DI
08058056681751 FDA UDI
FDA Product Code
KQN FDA UDI
GMDN Term
Angiotensin converting enzyme (ACE) IVD, reagent FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1090 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Total Volume — 40 Milliliter FDA UDI

Category: Angiotensin converting enzyme (ACE) IVD, reagent

ACE Liquid by Sentinel Ch. Srl — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Angiotensin converting enzyme (ACE) IVD, reagent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sentinel Ch. Srl

Sources (1)

  • FDA UDI d23658f2-b274-4164-9f31-5427d91869b6 37 fields · synced May 31, 2026