eCHO Basal Medium Powder - 200L

FDA UDI

Class I (US FDA UDI)

by Lonza Verviers

Identity

Trade Name: eCHO Basal Medium Powder - 200L FDA UDI
Generic Name: Ex vivo cell culture medium FDA UDI
Model / Reference: BE15-933Q FDA UDI

Identifiers

Catalog Number: BE15-933Q FDA UDI
Primary DI / UDI-DI: 05407010123654 FDA UDI
FDA Product Code: KIT FDA UDI
GMDN Term: Ex vivo cell culture medium 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Ex vivo cell culture medium

eCHO Basal Medium Powder - 200L by Lonza Verviers — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Lonza Verviers

Sources (1)

FDA UDI b90e66c7-6c65-41c6-b5c4-010446e808ea 33 fields · synced May 31, 2026