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Curaplex

FDA UDI

Class II (US FDA UDI)

by Bound Tree Medical, Llc

Identity

Trade Name
Curaplex FDA UDI
Generic Name
Nasogastric feeding tube FDA UDI
Device Name
Curaplex Nasogastric Tube, 10Fr 280ea/cs FDA UDI
Model / Reference
14757MS FDA UDI
Description
Curaplex Nasogastric Tube, 10Fr 280ea/cs FDA UDI

Identifiers

Primary DI / UDI-DI
00817617022314 FDA UDI
FDA Product Code
KNT FDA UDI
GMDN Term
Nasogastric feeding tube FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5980 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

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Dimensions & Sizes

Size
Catheter Gauge — 10 French FDA UDI

Category: Nasogastric feeding tube

The Curaplex Nasogastric Tube is a sterile, thin, flexible, hollow cylinder with a single lumen, rubber or plastic, used for enteral feeding and medication administration.

Similar devices

Also classified as Nasogastric feeding tube.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI be139f2b-3dac-450f-b6a5-adb5ff5e2b4b 34 fields · synced Jun 19, 2026