FDA UDI In Commercial Distribution 🇺🇸 United States

Panoscreen I and II

DI: 10888234000327 · Model: 0002390 · IMMUCOR, INC.
Product Codes
0
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Panoscreen I and II
Primary DI
10888234000327
Version / Model
0002390
Catalog Number
0002390
Company Name
IMMUCOR, INC.
Labeler DUNS
061446282
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-24
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
eb299c68-ce25-4f69-88a2-aa73d6f5e999

Device Description

This product is used in the detection of unexpected red blood cell blood group antibodies. This product is a two (2) vial set, with each vial containing a 2 - 4% reagent red blood cell suspension of a unique group O donor of known antigen make-up.

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
Yes
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

GMDN Terms

Code Name
52544 Antibody screening reagent red blood cell IVD, kit, agglutination

Identifiers

Type ID
Primary 10888234000327

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
1 – 10 Degrees Celsius