FDA UDI Not in Commercial Distribution 🇺🇸 United States

GEM Test ACT+ Cartridges

DI: 08426950088585 · Model: 06260038000 · INSTRUMENTATION LABORATORY COMPANY
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
45

Basic Information

Brand Name
GEM Test ACT+ Cartridges
Primary DI
08426950088585
Version / Model
06260038000
Catalog Number
06260038000
Company Name
INSTRUMENTATION LABORATORY COMPANY
Labeler DUNS
557223252
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
45
Record Status
Published
Publish Date
2016-09-23
Public Version
6
Public Version Date
2024-01-26
Public Version Status
Update
Public Device Record Key
d243439c-04fb-4532-ad63-3a33bbeeef32
Distribution End Date
2024-01-25

Device Description

GEM Test ACT+ Cartridges

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
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
55993 Activated clotting time (ACT) IVD, kit, clotting

Identifiers

Type ID
Primary 08426950088585
Unit of Use 18426950088582

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 8 Degrees Celsius