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Grip-Lok

FDA UDI

Class I (US FDA UDI)

by Tidi Products, Llc

Identity

Trade Name
Grip-Lok FDA UDI
Generic Name
Wearable percutaneous catheter/tube holder FDA UDI
Device Name
Medium Peripheral IV and Arterial Securement Device and Dressing Kit FDA UDI
Model / Reference
3300MART-KIT-2 FDA UDI
Description
Medium Peripheral IV and Arterial Securement Device and Dressing Kit FDA UDI

Identifiers

Catalog Number
3300MART-KIT-2 FDA UDI
Primary DI / UDI-DI
00618125177097 FDA UDI
FDA Product Code
KMK FDA UDI
GMDN Term
Wearable percutaneous catheter/tube holder FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5210 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

Yes

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: Wearable percutaneous catheter/tube holder

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

Similar devices

Also classified as Wearable percutaneous catheter/tube holder.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Tidi Products, Llc

Sources (1)

  • FDA UDI ed40ba3a-5fb5-4859-ba8f-b0d0f7397df0 34 fields · synced May 30, 2026