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Mini Wright

FDA UDI

Class II (US FDA UDI)

by Clement Clarke International Limited

Identity

Trade Name
Mini Wright FDA UDI
Generic Name
Peak flow meter, manual FDA UDI
Device Name
MW STD ATS (MEDLINE) SINGLE FDA UDI
Model / Reference
3103842S FDA UDI
Description
MW STD ATS (MEDLINE) SINGLE FDA UDI

Identifiers

Catalog Number
3103842S FDA UDI
Primary DI / UDI-DI
05023323001450 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

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Peak flow meter, manual

Mini Wright by Clement Clarke International Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peak flow meter, manual.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6d2c73fd-3f23-4494-b189-554e440e554c 35 fields · synced May 30, 2026