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Catheter Stabilization Device

FDA UDI

Class I (US FDA UDI)

by C. R. Bard, Inc.

Identity

Trade Name
Catheter Stabilization Device FDA UDI
Generic Name
Nasogastric tube holder, noninvasive FDA UDI
Device Name
StatLock Nasogastric Stabilization Devices, Catheter Stabilization Device, adult pad, includes skin prep pad FDA UDI
Model / Reference
NG0120 FDA UDI
Description
StatLock Nasogastric Stabilization Devices, Catheter Stabilization Device, adult pad, includes skin prep pad FDA UDI

Identifiers

Catalog Number
NG0120 FDA UDI
Primary DI / UDI-DI
10801741076173 FDA UDI
FDA Product Code
KMK FDA UDI
GMDN Term
Nasogastric tube holder, noninvasive 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

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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: Nasogastric tube holder, noninvasive

Catheter Stabilization Device by C. R. Bard, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nasogastric tube holder, noninvasive.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
C. R. Bard, Inc.

Sources (1)

  • FDA UDI e6efdb08-5998-4840-a1ff-cd810367ded7 35 fields · synced Jun 1, 2026