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Curaplex

FDA UDI

Class I (US FDA UDI)

by Tri-Anim Health Services, Inc.

Identity

Trade Name
Curaplex FDA UDI
Generic Name
Nose clip, single-use FDA UDI
Device Name
NOSECLIP,OVERSIZED50/BG FDA UDI
Model / Reference
301-PFR52NC FDA UDI
Description
NOSECLIP,OVERSIZED50/BG FDA UDI

Identifiers

Primary DI / UDI-DI
00812574023817 FDA UDI
FDA Product Code
BXJ FDA UDI
GMDN Term
Nose clip, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.6225 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

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Nose clip, single-use

Curaplex by Tri-Anim Health Services, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nose clip, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 41c31597-4684-4cbe-aad4-5734785c9498 33 fields · synced Jun 8, 2026