← Back to catalogue

Grip-Lok

FDA UDI

Class I (US FDA UDI)

by Tidi Products, Llc

Identity

Trade Name
Grip-Lok FDA UDI
Generic Name
Urinary catheter holder FDA UDI
Device Name
Large Foley Catheter Securement Device for 2 & 3 way Foley Catheters sized 8 - 30 Fr FDA UDI
Model / Reference
3400LFC-10PK FDA UDI
Description
Large Foley Catheter Securement Device for 2 & 3 way Foley Catheters sized 8 - 30 Fr FDA UDI

Identifiers

Catalog Number
3400LFC-10PK FDA UDI
Primary DI / UDI-DI
10618125192172 FDA UDI
FDA Product Code
EYJ FDA UDI
GMDN Term
Urinary catheter holder FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.5130 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Urinary catheter holder

Grip-Lok by Tidi Products, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Urinary catheter holder.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Tidi Products, Llc

Sources (1)

  • FDA UDI 44315158-eebf-4469-8624-7da3da53cdea 34 fields · synced Jun 6, 2026