FDA UDI In Commercial Distribution 🇺🇸 United States

GBX Developer and Replenisher

DI: 40889971900988 · Model: GBX Developer and Replenisher · CARESTREAM HEALTH, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
GBX Developer and Replenisher
Primary DI
40889971900988
Version / Model
GBX Developer and Replenisher
Catalog Number
1900984
Company Name
CARESTREAM HEALTH, INC.
Labeler DUNS
793169512
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-16
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
22296e31-48d9-4fc5-9863-0269b6b1b3aa

Device Description

GBX DEVELOPER AND REPL 19L

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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
IWZ Film, radiographic

GMDN Terms

Code Name
41008 X-ray film processing chemical, manual

Identifiers

Type ID
Package 60889971900982
Primary 40889971900988