FDA UDI In Commercial Distribution 🇺🇸 United States

CELLEX

DI: 00705030000050 · Model: CLXUSA · Therakos LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CELLEX
Primary DI
00705030000050
Version / Model
CLXUSA
Catalog Number
CLXUSA
Company Name
Therakos LLC
Labeler DUNS
003083703
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-11-07
Public Version
2
Public Version Date
2026-04-24
Public Version Status
Update
Public Device Record Key
73fbeb56-d45c-4ec5-96e1-c2ade9ae182c

Device Description

Cellex Procedural Kit U.S.

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
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
LNR System, Photopheresis, Extracorporeal

GMDN Terms

Code Name
46913 Photopheresis system blood set

Identifiers

Type ID
Primary 00705030000050

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-20 – 50 Degrees Celsius