FDA UDI In Commercial Distribution 🇺🇸 United States

LANEX Medium Screens

DI: 60889978472345 · Model: LANEX Medium Screens · CARESTREAM HEALTH, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
20

Basic Information

Brand Name
LANEX Medium Screens
Primary DI
60889978472345
Version / Model
LANEX Medium Screens
Catalog Number
8472342
Company Name
CARESTREAM HEALTH, INC.
Labeler DUNS
793169512
Distribution Status
In Commercial Distribution
Device Count in Pkg
20
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
21180a83-e3c1-4fcf-b5c4-36e3b8405a27

Device Description

20PR 18X24CM LANEX MED C2 W/O FOAM

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
EAM Screen, intensifying, radiographic

GMDN Terms

Code Name
34317 X-ray intensifying screen

Identifiers

Type ID
Primary 60889978472345
Unit of Use 00889978472343

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
10 – 24 Degrees Celsius