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T8006 Sensititre™ Cation Adjusted Mueller-Hinton w/ TES w/ OADC

FDA UDI

Class II (US FDA UDI)

by Remel, Inc.

Identity

Trade Name
T8006 Sensititre™ Cation Adjusted Mueller-Hinton w/ TES w/ OADC FDA UDI
Generic Name
Mueller-Hinton broth antimicrobial susceptibility culture medium IVD FDA UDI
Model / Reference
T8006 Sensititre™ Cation Adjusted Mueller-Hinton w/ TES w/ OADC FDA UDI

Identifiers

Primary DI / UDI-DI
00848838090981 FDA UDI
FDA Product Code
JTZ FDA UDI
GMDN Term
Mueller-Hinton broth antimicrobial susceptibility culture medium IVD 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

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Mueller-Hinton broth antimicrobial susceptibility culture medium IVD

T8006 Sensititre™ Cation Adjusted Mueller-Hinton w/ TES w/ OADC by Remel, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Mueller-Hinton broth antimicrobial susceptibility culture medium IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Remel, Inc.

Sources (1)

  • FDA UDI fd16cba1-4560-4bc8-b233-dda6c2c59e10 32 fields · synced May 30, 2026