FDA UDI In Commercial Distribution 🇺🇸 United States

FlexGRIP

DI: 05430003674130 · Model: FlexGRIP Jr. NEX · Bedal
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
FlexGRIP
Primary DI
05430003674130
Version / Model
FlexGRIP Jr. NEX
Catalog Number
NEXJR
Company Name
Bedal
Labeler DUNS
370066406
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-12-02
Public Version
1
Public Version Date
2025-12-10
Public Version Status
New
Public Device Record Key
ca74e463-4ebb-4cd9-9725-a6d954b1a221

Device Description

Sterilized Product

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Conditional
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
58301 Synthetic polymer semi-permeable film dressing, adhesive

Identifiers

Type ID
Package 05430003674147
Primary 05430003674130
Package 05430003674154

Customer Contacts

Phone
+3211286902

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
10 – 30 Degrees Celsius
Type
Storage Environment Temperature
Temperature Range
50 – 86 Degrees Fahrenheit