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Flotec

FDA UDI

Class I (US FDA UDI)

by Flotec, Inc.

Identity

Trade Name
Flotec FDA UDI
Generic Name
Medical gas flowmeter, dial-type FDA UDI
Model / Reference
Flowmeter FDA UDI

Identifiers

Primary DI / UDI-DI
B741FM0 FDA UDI
FDA Product Code
BXY FDA UDI
GMDN Term
Medical gas flowmeter, dial-type FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.2350 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Medical gas flowmeter, dial-type

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

Similar devices

Also classified as Medical gas flowmeter, dial-type.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Flotec, Inc.

Sources (1)

  • FDA UDI 50b82ae2-9829-492f-92b5-015bcc22585b 33 fields · synced May 30, 2026