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Pxp-Lavare

FDA UDI

Class II (US FDA UDI)

by Thermogenesis Corp.

Identity

Trade Name
PXP-LAVARE FDA UDI
Generic Name
Blood centrifugation system containment kit FDA UDI
Device Name
PXP-LAVARE Docking Station, packaged FDA UDI
Model / Reference
80122 FDA UDI
Description
PXP-LAVARE Docking Station, packaged FDA UDI

Identifiers

Primary DI / UDI-DI
00886368000223 FDA UDI
FDA Product Code
OAO FDA UDI
GMDN Term
Blood centrifugation system containment kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.9900 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

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Blood centrifugation system containment kit

Pxp-Lavare by Thermogenesis Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood centrifugation system containment kit.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Thermogenesis Corp.

Sources (1)

  • FDA UDI 3be848a3-c8da-46ba-bae5-3689dec60525 36 fields · synced May 30, 2026