← Back to catalogue
Microtest M4rt (3ml) W/O Beads Tube, Red Pk/72
EUDAMEDFDA UDIClass A (EU MDR)
Ref R12700
by Remel, Inc.
Identity
- Trade Name
- MICROTEST M4RT (3ML) W/O BEADS TUBE, RED PK/72 EUDAMEDMicroTest M4RT FDA UDI
- Generic Name
- Microbiological transport medium IVD FDA UDI
- Device Name
- MICROTEST M4RT EUDAMEDM4RT(3ml) w/o beads PK/72 FDA UDI
- Model / Reference
- R12700 EUDAMEDFDA UDI
- Description
- M4RT(3ml) w/o beads PK/72 FDA UDI
Identifiers
- Catalog Number
- R12700 FDA UDI
- Primary DI / UDI-DI
- 00842558108919 EUDAMEDFDA UDI
- Basic UDI-DI
- 8488380M4RTA3 EUDAMED
- 510(k) Number
- K965152 FDA UDI
- FDA Product Code
- JSM FDA UDI
- EMDN Code
- W0104010203 TRANSPORT MEDIA EUDAMED
- GMDN Term
- Microbiological transport medium IVD FDA UDI
Classification
- Device Class
- Class A EUDAMEDClass I FDA UDI
- Regulation Number
- 866.2390 FDA UDI
- Market of Registration
- Netherlands EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Human Tissues
No
EUDAMED
Animal Tissues
Yes
EUDAMED
Microbial Substances
No
EUDAMED
Reagent
Yes
EUDAMED
Self Testing
No
EUDAMED
Near-Patient Testing
No
EUDAMED
Professional Testing
Yes
EUDAMED
Companion Diagnostics
No
EUDAMED
Surgical Instrument
No
EUDAMED
New Device
No
EUDAMED
Prescription Use
No
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
Microtest M4rt (3ml) W/O Beads Tube, Red Pk/72 by Remel, Inc. — Class A — IVDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/IVDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDR | 8488380M4RTA3 | Class A | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class A | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Remel, Inc.
- EUDAMED SRN
- US-MF-000044686
- Authorised Representative
- Thermo Fisher Diagnostics B.V. NL-AR-000013157
Sources (2)
- EUDAMED 52aaf59a-d0ae-4302-ba6e-9963d2413fde 61 fields · synced Jun 19, 2026
- FDA UDI 47e5dde0-2a67-4e4b-b25f-7722cfe12caf 35 fields · synced May 30, 2026