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Perfadex with THAM

FDA UDI

Class II (US FDA UDI)

by Xvivo Perfusion, Inc.

Identity

Trade Name
Perfadex with THAM FDA UDI
Generic Name
Donor-organ/tissue/cell preservation solution FDA UDI
Device Name
Perfadex® Solution for Lung Perfusion is indicated for the flushing, storage and transportation of isolated lungs after removal from the donor in preparation for eventual transplantation into a recipient. Package size 2 x 2800 ml FDA UDI
Model / Reference
19018 FDA UDI
Description
Perfadex® Solution for Lung Perfusion is indicated for the flushing, storage and transportation of isolated lungs after removal from the donor in preparation for eventual transplantation into a recipient. Package size 2 x 2800 ml FDA UDI

Identifiers

Catalog Number
19018 FDA UDI
Primary DI / UDI-DI
07350069520067 FDA UDI
FDA Product Code
KDN FDA UDI
GMDN Term
Donor-organ/tissue/cell preservation solution FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5880 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Perfadex with THAM by Xvivo Perfusion, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7ec69c5b-9709-46af-a6f9-c34434d8f6b6 37 fields · synced Jun 20, 2026