← Back to catalogue

Curad

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Curad FDA UDI
Generic Name
Nasogastric tube holder, noninvasive FDA UDI
Device Name
FASTENER,NASAL TUBE,ADULT,TAN,50/BX FDA UDI
Model / Reference
CURNASTUB50 FDA UDI
Description
FASTENER,NASAL TUBE,ADULT,TAN,50/BX FDA UDI

Identifiers

Catalog Number
CURNASTUB50 FDA UDI
Primary DI / UDI-DI
80884389113362 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

Dimensions & Sizes

Size
Width — 1.75 Inch FDA UDI
Length — 2.125 Inch FDA UDI

Category: Nasogastric tube holder, noninvasive

Curad by Medline Industries, 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

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

Manufacturer

Sources (1)

  • FDA UDI b3983825-a754-43b7-862e-76183edd3d0a 36 fields · synced May 30, 2026