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Flow-Safe Anti-Asphyxia Valve Elbow

FDA UDI

Class II (US FDA UDI)

by Mercury Enterprises, Inc.

Identity

Trade Name
Flow-Safe Anti-Asphyxia Valve Elbow FDA UDI
Generic Name
Ventilator breathing circuit, single-use FDA UDI
Device Name
For use with Flow-Safe, Flow-Safe II, Flow-Safe IIEZ FDA UDI
Model / Reference
10-57121 FDA UDI
Description
For use with Flow-Safe, Flow-Safe II, Flow-Safe IIEZ FDA UDI

Identifiers

Primary DI / UDI-DI
10641043571217 FDA UDI
510(k) Number
K090710 FDA UDI
FDA Product Code
BYE FDA UDI
GMDN Term
Ventilator breathing circuit, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5965 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

Yes

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

No

FDA UDI

Category: Ventilator breathing circuit, single-use

Flow-Safe Anti-Asphyxia Valve Elbow by Mercury Enterprises, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ventilator breathing circuit, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7444bf73-2ff1-4bdd-af32-1a4c16748738 35 fields · synced Jun 1, 2026