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Select

FDA UDI

Class I (US FDA UDI)

by Bio-Rad

Identity

Trade Name
Select FDA UDI
Generic Name
Differential/selective agar culture medium IVD FDA UDI
Device Name
CandiSelect FDA UDI
Model / Reference
63740 FDA UDI
Description
CandiSelect FDA UDI

Identifiers

Catalog Number
63740 FDA UDI
Primary DI / UDI-DI
03610520034309 FDA UDI
FDA Product Code
JSH FDA UDI
GMDN Term
Differential/selective agar culture medium IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.2320 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Differential/selective agar culture medium IVD

Select by Bio-Rad — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Differential/selective agar culture medium IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bio-Rad

Sources (1)

  • FDA UDI 4c83132f-e4a5-4add-bc0b-8a8af2505206 37 fields · synced Jun 8, 2026