FDA UDI In Commercial Distribution 🇺🇸 United States

HemosIL AcuStar System Rinse

DI: 08426950497035 · Model: 0009802200 · INSTRUMENTATION LABORATORY COMPANY
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
HemosIL AcuStar System Rinse
Primary DI
08426950497035
Version / Model
0009802200
Catalog Number
0009802200
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
5
Public Version Date
2021-07-14
Public Version Status
Update
Public Device Record Key
bdd834f5-dd92-4aca-a638-89dee8c5794c

Device Description

HemosIL AcuStar System Rinse

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
Yes
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
JPA SYSTEM, MULTIPURPOSE FOR IN VITRO COAGULATION STUDIES

GMDN Terms

Code Name
59058 Wash/cleaning solution IVD, automated/semi-automated system

Identifiers

Type ID
Primary 08426950497035

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 25 Degrees Celsius