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NeoGrip®

FDA UDI

Class I (US FDA UDI)

by Neotech Products LLC

Identity

Trade Name
NeoGrip® FDA UDI
Generic Name
Wearable percutaneous catheter/tube holder FDA UDI
Device Name
The NeoGrip/VersaGrip is intended to organize tubes, cables and circuits. FDA UDI
Model / Reference
Assorted FDA UDI
Description
The NeoGrip/VersaGrip is intended to organize tubes, cables and circuits. FDA UDI

Identifiers

Catalog Number
N602A FDA UDI
Primary DI / UDI-DI
00812594012471 FDA UDI
FDA Product Code
JAY FDA UDI
GMDN Term
Wearable percutaneous catheter/tube holder FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5280 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

Yes

FDA UDI

Category: Wearable percutaneous catheter/tube holder

NeoGrip® by Neotech 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

Sources (1)

  • FDA UDI c3cce26c-f74c-4d45-a1e7-d14f288edf32 34 fields · synced Jun 1, 2026