FDA UDI Not in Commercial Distribution 🇺🇸 United States

CathGrip

DI: 00653599000717 · Model: 54002 · BIODERM, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
CathGrip
Primary DI
00653599000717
Version / Model
54002
Company Name
BIODERM, INC.
Labeler DUNS
114773653
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-01-07
Public Version
2
Public Version Date
2023-04-07
Public Version Status
Update
Public Device Record Key
2ba008b5-cea3-4263-a728-552e935d2d87
Distribution End Date
2023-04-06

Device Description

CathGrip Oval, Small, Sterile

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

Identifiers

Type ID
Package 10653599000714
Primary 00653599000717
Secondary M456540020

Customer Contacts

Phone
800-814-3174

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
10 – 30 Degrees Celsius