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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 Umbilical Venous Catheterization Kit FDA UDI
Model / Reference
12186 FDA UDI
Description
Curaplex Umbilical Venous Catheterization Kit FDA UDI

Identifiers

Catalog Number
12186 FDA UDI
Primary DI / UDI-DI
00815277020084 FDA UDI
FDA Product Code
FMF FDA UDI
POQ FDA UDI
KDH FDA UDI
GMDN Term
Nasogastric feeding tube FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5860 FDA UDI
880.5440 FDA UDI
876.5980 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: General-purpose syringe, single-useNasogastric feeding tubeStopcockUmbilical cord tape

Curaplex by Bound Tree Medical, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Antiseptic skin towelette.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bound Tree Medical, Llc

Sources (1)

  • FDA UDI 4f265f79-5d7f-4050-b9ae-072090771641 34 fields · synced Jun 1, 2026