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Shanghai Beijin

FDA UDI

Class I (US FDA UDI)

by Shanghai Beijin Biotechnological Co., LTD

Identity

Trade Name
Shanghai Beijin FDA UDI
Generic Name
Cell culture medium IVD FDA UDI
Device Name
EDEN BASAL MEDIUM FDA UDI
Model / Reference
EDEN BASAL MEDIUM FDA UDI
Description
EDEN BASAL MEDIUM FDA UDI

Identifiers

Primary DI / UDI-DI
06975756090008 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

No

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Cell culture medium IVD

Shanghai Beijin by Shanghai Beijin Biotechnological Co., LTD — 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 1d6c68f3-4348-4490-b0fc-872494c46528 33 fields · synced May 30, 2026