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InTray® MSA

FDA UDI

Class I (US FDA UDI)

by Biomed Diagnostics, Inc.

Identity

Trade Name
InTray® MSA FDA UDI
Generic Name
Mannitol-salt Staphylococcus species agar culture medium IVD FDA UDI
Device Name
Mannitol Salt Agar (MSA) test uses a selective isolation media for the enumeration of staphylococci from clinical/non-clinical materials. A change of the phenol red indicator (Mannitol fermentation) aids in differentiating staphylococci species. FDA UDI
Model / Reference
1303 FDA UDI
Description
Mannitol Salt Agar (MSA) test uses a selective isolation media for the enumeration of staphylococci from clinical/non-clinical materials. A change of the phenol red indicator (Mannitol fermentation) aids in differentiating staphylococci species. FDA UDI

Identifiers

Catalog Number
21-303-001 FDA UDI
Primary DI / UDI-DI
B08813030 FDA UDI
FDA Product Code
JSI FDA UDI
GMDN Term
Mannitol-salt Staphylococcus species agar culture medium IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.2360 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

No

FDA UDI

Category: Mannitol-salt Staphylococcus species agar culture medium IVD

InTray® MSA by Biomed Diagnostics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5d1f6013-4244-4346-83c4-63ad364e1e7e 35 fields · synced May 29, 2026