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Bag Tee For Mxr & Std Flmr, Ce

FDA UDI

Class I (US FDA UDI)

by Parker Hannifin Corp.

Identity

Trade Name
BAG TEE FOR MXR & STD FLMR, CE FDA UDI
Generic Name
Non-rebreathing valve, reusable FDA UDI
Device Name
BAG TEE FOR MXR & STD FLMR, CE FDA UDI
Model / Reference
P1407E FDA UDI
Description
BAG TEE FOR MXR & STD FLMR, CE FDA UDI

Identifiers

Catalog Number
P1407E FDA UDI
Primary DI / UDI-DI
00816711020394 FDA UDI
FDA Product Code
BTC FDA UDI
GMDN Term
Non-rebreathing valve, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5320 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

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Non-rebreathing valve, reusable

Bag Tee For Mxr & Std Flmr, Ce by Parker Hannifin Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Non-rebreathing valve, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6b0b9348-b33d-40f3-b732-d7506265e083 34 fields · synced May 30, 2026