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Tobramycin ONLINE TDM Tobramycin

FDA UDI

Class II (US FDA UDI)

by Roche Diagnostics Corp.

Identity

Trade Name
Tobramycin ONLINE TDM Tobramycin FDA UDI
Generic Name
Tobramycin therapeutic drug monitoring IVD, kit, enzyme immunoassay (EIA) FDA UDI
Model / Reference
4642503190 FDA UDI

Identifiers

Catalog Number
4642503190 FDA UDI
Primary DI / UDI-DI
04015630997930 FDA UDI
510(k) Number
K060853 FDA UDI
FDA Product Code
KLB FDA UDI
GMDN Term
Tobramycin therapeutic drug monitoring IVD, kit, enzyme immunoassay (EIA) FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.3900 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

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Tobramycin ONLINE TDM Tobramycin by Roche Diagnostics Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f65fe33b-6afe-4a8c-984d-d2f91a7525be 36 fields · synced Jun 6, 2026