FDA UDI Not in Commercial Distribution 🇺🇸 United States

Kit Control

DI: 10888234500322 · Model: 403591 · IMMUCOR GTI DIAGNOSTICS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Kit Control
Primary DI
10888234500322
Version / Model
403591
Catalog Number
403591
Company Name
IMMUCOR GTI DIAGNOSTICS, INC.
Labeler DUNS
606034197
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-07-08
Public Version
4
Public Version Date
2018-08-01
Public Version Status
Update
Public Device Record Key
22a1fdc8-22ba-48df-8412-38e76925bb38
Distribution End Date
2018-08-01

Device Description

For Use with Factor VIII Antibody Screen

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
GGP Test, Qualitative And Quantitative Factor Deficiency

GMDN Terms

Code Name
57053 Coagulation factor VIII-associated antigen IVD, kit, enzyme immunohistochemistry

Identifiers

Type ID
Primary 10888234500322

Customer Contacts

Phone
855-466-8267

Premarket Submissions

Submission Number Supplement Number
K082205 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 8 Degrees Celsius