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Flotec

FDA UDI

Class I (US FDA UDI)

by Flotec, Inc.

Identity

Trade Name
Flotec FDA UDI
Generic Name
High-pressure medical gas hose FDA UDI
Model / Reference
Mass Casualty Assembly FDA UDI

Identifiers

Primary DI / UDI-DI
B741MC0 FDA UDI
FDA Product Code
BYX FDA UDI
GMDN Term
High-pressure medical gas hose FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5860 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

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Non-fixed medical gas cylinder regulatorMedical gas flowmeter, dial-typeHigh-pressure medical gas hose

Flotec by Flotec, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as High-pressure medical gas hose.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Flotec, Inc.

Sources (1)

  • FDA UDI 9e53fe00-46d9-4731-bfda-7bc197c4c934 33 fields · synced Jun 1, 2026