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Rotationsflowgeber Set

FDA UDI

Class II (US FDA UDI)

by eResearchTechnology, Inc.

Identity

Trade Name
Rotationsflowgeber Set FDA UDI
Generic Name
Expiratory peak flow meter, digital FDA UDI
Device Name
Set of three rotary flow sensors for single-patient use, accessory to Asthma Monitor FDA UDI
Model / Reference
Rotationsflowgeber Set FDA UDI
Description
Set of three rotary flow sensors for single-patient use, accessory to Asthma Monitor FDA UDI

Identifiers

Primary DI / UDI-DI
04057155000320 FDA UDI
510(k) Number
K090486 FDA UDI
K092890 FDA UDI
K133722 FDA UDI
FDA Product Code
BZG FDA UDI
GMDN Term
Expiratory peak flow meter, digital FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.1840 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Expiratory peak flow meter, digital

Rotationsflowgeber Set by eResearchTechnology, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Expiratory peak flow meter, digital.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4d9a587c-c03e-48df-bf72-217ab15c9b59 35 fields · synced May 30, 2026