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Select

FDA UDI

Class II (US FDA UDI)

by Bio-Rad

Identity

Trade Name
Select FDA UDI
Generic Name
MRSA agar culture medium IVD, chromogenic FDA UDI
Device Name
MRSASelectTM II - 100 tests FDA UDI
Model / Reference
63763 FDA UDI
Description
MRSASelectTM II - 100 tests FDA UDI

Identifiers

Primary DI / UDI-DI
03610521536215 FDA UDI
510(k) Number
K171061 FDA UDI
FDA Product Code
JSO FDA UDI
GMDN Term
MRSA agar culture medium IVD, chromogenic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.1700 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

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

Category: MRSA agar culture medium IVD, chromogenic

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

Similar devices

Also classified as MRSA agar culture medium IVD, chromogenic.

Cleared under the same submission

K171061 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bio-Rad

Sources (1)

  • FDA UDI 1a4056ff-ebe0-482a-80e6-0fbebb9da0bd 37 fields · synced Jun 8, 2026