← Back to catalogue

Belzer MPS (UW Machine Perfusion Solution )

FDA UDI

Class II (US FDA UDI)

by Preservation Solutions, Inc.

Identity

Trade Name
Belzer MPS (UW Machine Perfusion Solution ) FDA UDI
Generic Name
Donor-organ/tissue/cell preservation solution FDA UDI
Device Name
Formulated for the in-vitro flushing and continuous hypothermic machine perfusion preservation of explanted kidneys. 1000 mL FDA UDI
Model / Reference
BTLBMPS-1000 FDA UDI
Description
Formulated for the in-vitro flushing and continuous hypothermic machine perfusion preservation of explanted kidneys. 1000 mL FDA UDI

Identifiers

Primary DI / UDI-DI
00810805000101 FDA UDI
510(k) Number
K080432 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
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

Dimensions & Sizes

Size
Total Volume — 1000 Milliliter FDA UDI

Category: Donor-organ/tissue/cell preservation solution

Belzer MPS (UW Machine Perfusion Solution ) by Preservation Solutions, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Donor-organ/tissue/cell preservation solution.

Cleared under the same submission

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 97342a37-9b7a-43bc-9d80-1e239a4c7906 36 fields · synced May 30, 2026