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Qflow

FDA UDIEUDAMED

Class II (US FDA UDI)

by FIM Medical

Identity

Trade Name
QFLOW FDA UDI
Generic Name
Pulmonary function testing filter/mouthpiece FDA UDI
Model / Reference
QFLOW FDA UDI

Identifiers

Primary DI / UDI-DI
03760253450331 FDA UDI
510(k) Number
K161676 FDA UDI
FDA Product Code
BZG FDA UDI
GMDN Term
Pulmonary function testing filter/mouthpiece 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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Pulmonary function testing filter/mouthpiece

Qflow by FIM Medical — Class II — MDD, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Pulmonary function testing filter/mouthpiece.

Cleared under the same submission

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDD

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
FIM Medical

Sources (2)

  • FDA UDI 37e50cfc-ab48-4c7e-90ef-f23903d8dc9a 34 fields · synced Jun 17, 2026
  • EUDAMED 1 fields · synced Jun 2, 2026