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Med Matrx Scav W/Scv, 3l Bag

FDA UDI

Class I (US FDA UDI)

by Parker Hannifin Corp.

Identity

Trade Name
MED MATRX SCAV W/SCV, 3L BAG FDA UDI
Generic Name
Anaesthesia breathing circuit, reusable FDA UDI
Device Name
MED MATRX SCAV W/SCV, 3L BAG FDA UDI
Model / Reference
82502 FDA UDI
Description
MED MATRX SCAV W/SCV, 3L BAG FDA UDI

Identifiers

Catalog Number
82502 FDA UDI
Primary DI / UDI-DI
00816711021087 FDA UDI
FDA Product Code
KHA FDA UDI
GMDN Term
Anaesthesia breathing circuit, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5590 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Anaesthesia breathing circuit, reusable

Med Matrx Scav W/Scv, 3l Bag 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

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Manufacturer

Sources (1)

  • FDA UDI 3b03cd48-8fb4-4437-b20c-1a93d8cf007e 34 fields · synced Jun 1, 2026