FDA UDI In Commercial Distribution 🇺🇸 United States

CONTEX LF ST 4X5 10/CS

DI: 10612553013313 · Model: 50400000 · HARTMANN USA, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CONTEX LF ST 4X5 10/CS
Primary DI
10612553013313
Version / Model
50400000
Company Name
HARTMANN USA, INC.
Labeler DUNS
010137511
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-09-01
Public Version
2
Public Version Date
2024-01-29
Public Version Status
Update
Public Device Record Key
aaf4cf92-f2fb-4e95-9f2b-f571f31388d0

Device Description

CONTEX LF ST 4X5 10/CS

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FQM Bandage, Elastic

GMDN Terms

Code Name
10284 Pressure bandage, non-latex, single-use

Identifiers

Type ID
Primary 10612553013313