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Oral Surgery Bag Tee/Threaded

FDA UDI

Class I (US FDA UDI)

by Parker Hannifin Corp.

Identity

Trade Name
ORAL SURGERY BAG TEE/THREADED FDA UDI
Generic Name
Non-rebreathing valve, reusable FDA UDI
Device Name
ORAL SURGERY BAG TEE/THREADED FDA UDI
Model / Reference
P2407A FDA UDI
Description
ORAL SURGERY BAG TEE/THREADED FDA UDI

Identifiers

Catalog Number
P2407A FDA UDI
Primary DI / UDI-DI
00816711020844 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

Oral Surgery Bag Tee/Threaded 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 376644fc-ac20-4f64-b544-ead9ea026802 34 fields · synced May 30, 2026