← Back to catalogue

Matrx Scav, Shutoff Valve(wo/Ho

FDA UDI

Class I (US FDA UDI)

by Parker Hannifin Corp.

Identity

Trade Name
MATRX SCAV,SHUTOFF VALVE(WO/HO FDA UDI
Generic Name
Anaesthesia breathing circuit, reusable FDA UDI
Device Name
MATRX SCAV,SHUTOFF VALVE(WO/HO FDA UDI
Model / Reference
91515197 FDA UDI
Description
MATRX SCAV,SHUTOFF VALVE(WO/HO FDA UDI

Identifiers

Catalog Number
91515197 FDA UDI
Primary DI / UDI-DI
00816711021155 FDA UDI
FDA Product Code
CAI FDA UDI
GMDN Term
Anaesthesia breathing circuit, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5240 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Anaesthesia breathing circuit, reusable

Matrx Scav, Shutoff Valve(wo/Ho by Parker Hannifin Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Anaesthesia breathing circuit, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 14e72bd0-0c2d-4b11-a8b6-b98dcb06ebf7 34 fields · synced May 30, 2026