← Back to catalogue

Select

FDA UDI

Class II (US FDA UDI)

by Bio-Rad

Identity

Trade Name
Select FDA UDI
Generic Name
Differential/selective agar culture medium IVD FDA UDI
Device Name
MRSASelect FDA UDI
Model / Reference
63747 FDA UDI
Description
MRSASelect FDA UDI

Identifiers

Catalog Number
63747 FDA UDI
Primary DI / UDI-DI
03610520002933 FDA UDI
FDA Product Code
JSO FDA UDI
GMDN Term
Differential/selective agar culture medium IVD FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.1700 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Bio-Rad

Sources (1)

  • FDA UDI bf7d26e6-98c0-4990-a54d-2cb0bfb0d1f1 37 fields · synced May 30, 2026