FDA UDI In Commercial Distribution 🇺🇸 United States

ACE Calibrator

DI: 08058056681768 · Model: 1665001 · SENTINEL CH. SPA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ACE Calibrator
Primary DI
08058056681768
Version / Model
1665001
Catalog Number
1665001
Company Name
SENTINEL CH. SPA
Labeler DUNS
429572365
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-07-29
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
83c3b330-f06a-4dc4-a2f6-c88063bd002e

Device Description

ACE Calibrator is intended to be used with Sentinel ACE Liquid Reagent for the preparation of the calibration for the kinetic determination of angiotensin converting enzyme (ACE) assay in human serum or plasma. For In Vitro Diagnostic use.

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
JIT Calibrator, Secondary

GMDN Terms

Code Name
46015 Angiotensin converting enzyme (ACE) IVD, calibrator

Identifiers

Type ID
Primary 08058056681768

Customer Contacts

Phone
9999999999

Premarket Submissions

Submission Number Supplement Number
K141728 000

Device Sizes

Type Value Unit Text
Total Volume 3 Milliliter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store between 2 and 8 degrees Celsius