FDA UDI In Commercial Distribution 🇺🇸 United States

HemosIL AcuStar

DI: 08426950498001 · Model: 0009801000 · INSTRUMENTATION LABORATORY COMPANY
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
HemosIL AcuStar
Primary DI
08426950498001
Version / Model
0009801000
Catalog Number
0009801000
Company Name
INSTRUMENTATION LABORATORY COMPANY
Labeler DUNS
557223252
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
6
Public Version Date
2022-09-16
Public Version Status
Update
Public Device Record Key
5d30b966-2f2a-4438-89a7-cd09b91d3ee7

Device Description

ACL AcuStar

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
JPA SYSTEM, MULTIPURPOSE FOR IN VITRO COAGULATION STUDIES

GMDN Terms

Code Name
56689 Coagulation analyser IVD, laboratory

Identifiers

Type ID
Primary 08426950498001

Customer Contacts