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Zdan™

FDA UDI

Class I (US FDA UDI)

by Incell Corporation, Llc

Identity

Trade Name
ZDAN™ FDA UDI
Generic Name
Cell culture medium IVD FDA UDI
Device Name
A ZOICX Additive Sterile Filtered FDA UDI
Model / Reference
ZDAN04 FDA UDI
Description
A ZOICX Additive Sterile Filtered FDA UDI

Identifiers

Catalog Number
ZDAN04 FDA UDI
Primary DI / UDI-DI
G507ZDAN040 FDA UDI
FDA Product Code
KIT FDA UDI
GMDN Term
Cell culture medium IVD 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

Category: Cell culture medium IVD

Zdan™ by Incell Corporation, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cell culture medium IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 16dd64a4-f42c-4168-87ce-0ec18b9431fd 36 fields · synced May 30, 2026