FDA UDI In Commercial Distribution 🇺🇸 United States

RegenKit®-THT

DI: 07640138980770 · Model: 8495-9-001 · REGEN LAB SA
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
RegenKit®-THT
Primary DI
07640138980770
Version / Model
8495-9-001
Company Name
REGEN LAB SA
Labeler DUNS
482206518
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-15
Public Version
4
Public Version Date
2020-07-23
Public Version Status
Update
Public Device Record Key
d165761c-c13f-4675-8965-26d80b31f58f

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FMI Needle, Hypodermic, Single Lumen
FMF Syringe, Piston

GMDN Terms

Code Name
46923 Haematological concentrate system preparation kit, platelet concentration

Identifiers

Type ID
Primary 07640138980770

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
5 – 30 Degrees Celsius