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T-Piece, 22f, 22m, 22m With One-Way Valve

FDA UDI

Class I (US FDA UDI)

by Intersurgical Incorporated

Identity

Trade Name
T-PIECE, 22F, 22M, 22M WITH ONE-WAY VALVE FDA UDI
Generic Name
Non-rebreathing valve, single-use FDA UDI
Device Name
T-PIECE, 22F, 22M, 22M WITH ONE-WAY VALVE FDA UDI
Model / Reference
1952000 FDA UDI
Description
T-PIECE, 22F, 22M, 22M WITH ONE-WAY VALVE FDA UDI

Identifiers

Primary DI / UDI-DI
05030267057122 FDA UDI
FDA Product Code
BZA FDA UDI
GMDN Term
Non-rebreathing valve, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5810 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

Yes

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: Non-rebreathing valve, single-use

T-Piece, 22f, 22m, 22m With One-Way Valve by Intersurgical Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Non-rebreathing valve, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 51a1ddeb-d413-47ed-9433-83760e9dd905 34 fields · synced May 30, 2026