Curaplex

FDA UDI

Class II (US FDA UDI)

by Tri-Anim Health Services, Inc.

Identity

Trade Name: Curaplex FDA UDI
Generic Name: Peak flow meter, manual FDA UDI
Device Name: PEAK FLOW METER,CURAPLEX MINIWRIGHT,STANDARD FDA UDI
Model / Reference: 301-5900 FDA UDI
Description: PEAK FLOW METER,CURAPLEX MINIWRIGHT,STANDARD FDA UDI

Identifiers

Primary DI / UDI-DI: 00812574024371 FDA UDI
FDA Product Code: BZH FDA UDI
GMDN Term: Peak flow meter, manual FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 868.1860 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Peak flow meter, manual

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Tri-Anim Health Services, Inc.

Sources (1)

FDA UDI e9fb897c-9bbd-4593-a6b8-52eb73f6377e 33 fields · synced May 30, 2026