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Med-Rx

FDA UDI

Class II (US FDA UDI)

by Canadian Hospital Specialties Limited

Identity

Trade Name
MED-RX FDA UDI
Generic Name
Nasogastric feeding tube FDA UDI
Device Name
ENTERAL FEEDING TUBE, POLYURETHANE, 4 FR, FOR PEDIATRIC USE FDA UDI
Model / Reference
54-2440R FDA UDI
Description
ENTERAL FEEDING TUBE, POLYURETHANE, 4 FR, FOR PEDIATRIC USE FDA UDI

Identifiers

Catalog Number
54-2440R FDA UDI
Primary DI / UDI-DI
00628725002941 FDA UDI
510(k) Number
K100700 FDA UDI
FDA Product Code
FPD 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

No

FDA UDI

Category: Nasogastric feeding tube

Med-Rx by Canadian Hospital Specialties Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nasogastric feeding tube.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2bd5c730-c538-4af8-a35b-94a5942dae2a 36 fields · synced Jun 1, 2026