FDA UDI In Commercial Distribution 🇺🇸 United States

CathGrip

DI: 00653599001974 · Model: 51023NWCA · ARGENTUM MEDICAL, LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
CathGrip
Primary DI
00653599001974
Version / Model
51023NWCA
Company Name
ARGENTUM MEDICAL, LLC
Labeler DUNS
091449079
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-03-20
Public Version
4
Public Version Date
2025-11-20
Public Version Status
Update
Public Device Record Key
daed2cfe-916a-4a8d-a141-927cc920c73a

Device Description

CathGrip Single Strap, Extra Small, Sterile, No Wipes, Canada

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
Yes
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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KMK Device, Intravascular Catheter Securement

GMDN Terms

Code Name
56631 Wearable percutaneous catheter/tube holder, single-use

Identifiers

Type ID
Package 10653599001971
Primary 00653599001974
Package 00653599002292

Customer Contacts

Phone
800-864-6755

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
10 – 30 Degrees Celsius