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Cfas Myoglobin

FDA UDI

Class II (US FDA UDI)

by Roche Diagnostics Corp.

Identity

Trade Name
Cfas Myoglobin FDA UDI
Generic Name
Myoglobin IVD, calibrator FDA UDI
Model / Reference
4580044190 FDA UDI

Identifiers

Catalog Number
4580044190 FDA UDI
Primary DI / UDI-DI
04015630921300 FDA UDI
510(k) Number
K061683 FDA UDI
FDA Product Code
JIT FDA UDI
GMDN Term
Myoglobin IVD, calibrator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1150 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

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

Category: Myoglobin IVD, calibrator

Cfas Myoglobin by Roche Diagnostics Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Myoglobin IVD, calibrator.

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 b3ce23b5-b2d3-4287-a64d-f17be60a8f41 35 fields · synced May 30, 2026