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NG Strip™

FDA UDI

Class I (US FDA UDI)

by Derma Sciences Canada, Inc

Identity

Trade Name
NG Strip™ FDA UDI
Generic Name
Nasogastric tube holder, noninvasive FDA UDI
Device Name
Naso Gastric Strip. Nasal Tube Fastener with Dynamic Adherence FDA UDI
Model / Reference
NG-60 FDA UDI
Description
Naso Gastric Strip. Nasal Tube Fastener with Dynamic Adherence FDA UDI

Identifiers

Catalog Number
DERMA-NG60 FDA UDI
Primary DI / UDI-DI
10753567101600 FDA UDI
FDA Product Code
KGX FDA UDI
GMDN Term
Nasogastric tube holder, noninvasive FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5240 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Nasogastric tube holder, noninvasive

NG Strip™ by Derma Sciences Canada, 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

Sources (1)

  • FDA UDI 5ba13bab-28e0-4eea-8d94-f1bb5b2a43fa 35 fields · synced May 31, 2026