Walgreens

FDA UDI

Class II (US FDA UDI)

by Walgreen Co.

Identity

Trade Name: Walgreens FDA UDI
Generic Name: Inspiratory peak flow meter FDA UDI
Device Name: Walgreens Non-Digital Peak Flow Meter, single patient device to measure a patient's peak expiratory flow rate in liters/minutes FDA UDI
Model / Reference: 870981 FDA UDI
Description: Walgreens Non-Digital Peak Flow Meter, single patient device to measure a patient's peak expiratory flow rate in liters/minutes FDA UDI

Identifiers

Catalog Number: WIC 870981 FDA UDI
Primary DI / UDI-DI: 00311917047201 FDA UDI
510(k) Number: K101380 FDA UDI
FDA Product Code: BZH FDA UDI
GMDN Term: Inspiratory peak flow meter 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

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

FDA UDI

Category: Inspiratory peak flow meter

Walgreens by Walgreen Co. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Inspiratory peak flow meter.

Resp-O2 Peak Flow Meter Low Range 50-300 L/min — Dynarex Corp. · Class II
Resp-O2 Peak Flow Meter Full Range 50-800 L/min — Dynarex Corp. · Class II
Medline — MEDLINE INDUSTRIES, INC. · Class II

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: Walgreen Co.

Sources (1)

FDA UDI e3c9413e-0778-46ad-b4d0-6aed89412c99 36 fields · synced Jun 8, 2026