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Ez-Cpz-Nd™

FDA UDI

Class I (US FDA UDI)

by Incell Corporation, Llc

Identity

Trade Name
EZ-CPZ-ND™ FDA UDI
Generic Name
Donor-organ/tissue/cell preservation solution FDA UDI
Device Name
High Performance Cryopreservation Media and Storage Solution without DMSO FDA UDI
Model / Reference
EZND0500 FDA UDI
Description
High Performance Cryopreservation Media and Storage Solution without DMSO FDA UDI

Identifiers

Catalog Number
EZND0500 FDA UDI
Primary DI / UDI-DI
G507EZND05000 FDA UDI
FDA Product Code
KIT FDA UDI
GMDN Term
Donor-organ/tissue/cell preservation solution FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.2220 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Total Volume — 500 Milliliter FDA UDI

Category: Donor-organ/tissue/cell preservation solution

Ez-Cpz-Nd™ by Incell Corporation, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI aacc74e9-acea-498e-aa98-db2b940c523e 37 fields · synced May 30, 2026