FDA UDI In Commercial Distribution 🇺🇸 United States

Grip-Lok

DI: 00618125134823 · Model: 3301MCS-BD · TIDI PRODUCTS, LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Grip-Lok
Primary DI
00618125134823
Version / Model
3301MCS-BD
Catalog Number
3301MCS-BD
Company Name
TIDI PRODUCTS, LLC
Labeler DUNS
063519193
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-10-12
Public Version
1
Public Version Date
2022-10-20
Public Version Status
New
Public Device Record Key
13ea7390-772c-4202-88bd-7611d7dbbb0f

Device Description

Medium Securement Device for the BD Arterial Cannula with FloSwitch

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
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 10618125134820
Primary 00618125134823
Package 20618125134827