eudamed_udi
Primary ID: 00842558108919
MICROTEST M4RT (3ML) W/O BEADS TUBE, RED PK/72 (UDI 00842558108919)
Manufactured by Remel, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MICROTEST M4RT (3ML) W/O BEADS TUBE, RED PK/72 - Primary ID 00842558108919
Device Regulatory Overview
The MICROTEST M4RT (3ML) W/O BEADS TUBE, RED PK/72 (Model/Catalog Number: R12700) is a medical device manufactured by Remel, Inc.. This product is indexed under FDA Product Code / Category Classification W0104010203 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- R12700
- Product Code / EMDN
- W0104010203
- Device Name
- MICROTEST M4RT
- Database Sync Date
- 2026-08-09 16:51:21
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of MICROTEST M4RT (3ML) W/O BEADS TUBE, RED PK/72?
The registered manufacturer of record for MICROTEST M4RT (3ML) W/O BEADS TUBE, RED PK/72 is Remel, Inc..
What is the Primary UDI-DI identifier for MICROTEST M4RT (3ML) W/O BEADS TUBE, RED PK/72?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00842558108919.
What classification code is assigned to this device?
This device is registered under product classification code W0104010203.
Similar Classification Devices (W0104010203)
Other Devices by Remel, Inc.
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