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Patient Circuit

FDA UDI

Class II (US FDA UDI)

by Flight Medical Innovations Ltd

Identity

Trade Name
Patient Circuit FDA UDI
Generic Name
Ventilator breathing circuit, single-use FDA UDI
Device Name
F60 DL Autoclav Flow Sensor Kit(10pc) FDA UDI
Model / Reference
V64-0034 FDA UDI
Description
F60 DL Autoclav Flow Sensor Kit(10pc) FDA UDI

Identifiers

Primary DI / UDI-DI
17290013641011 FDA UDI
FDA Product Code
NOU FDA UDI
CBK FDA UDI
GMDN Term
Ventilator breathing circuit, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5895 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

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Ventilator breathing circuit, single-use

Patient Circuit by Flight Medical Innovations Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ventilator breathing circuit, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 122f5a58-8c58-43d3-8555-af365f5ad927 33 fields · synced May 31, 2026