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RAMP® Myoglobin TEST KIT +1 more model

FDA UDI

by Response Biomedical Corp

Identity

Trade Name
RAMP® Myoglobin TEST KIT; 25 TESTS FDA UDI
Generic Name
Myoglobin IVD, kit, rapid ICT, clinical FDA UDI
Model / Reference
C1103 FDA UDI

Identifiers

Primary DI / UDI-DI
10627966005022 FDA UDI
GMDN Term
Myoglobin IVD, kit, rapid ICT, clinical FDA UDI
Models / Variants
RAMP® Myoglobin TEST KIT FDA UDI
25 TESTS FDA UDI

Classification

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

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: Myoglobin IVD, kit, rapid ICT, clinical

RAMP® Myoglobin TEST KIT +1 more model by Response Biomedical Corp — FDA UDI — listed in FDA GUDID — 2 models — regulatory data on deviCERTS

Similar devices

Also classified as Myoglobin IVD, kit, rapid ICT, clinical.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Response Biomedical Corp

Sources (1)

  • FDA UDI 552e459d-1588-42e0-98a1-169fbf0ab739 32 fields · synced May 30, 2026