eudamed_udi
Primary ID: 00848838018350
MICROTEST M5 (3 ML) PK/72 (UDI 00848838018350)
Manufactured by Remel, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MICROTEST M5 (3 ML) PK/72 - Primary ID 00848838018350
Device Regulatory Overview
The MICROTEST M5 (3 ML) PK/72 (Model/Catalog Number: R12515) 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
- R12515
- Product Code / EMDN
- W0104010203
- Device Name
- MICROTEST M5
- Database Sync Date
- 2026-08-09 16:29:43
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 M5 (3 ML) PK/72?
The registered manufacturer of record for MICROTEST M5 (3 ML) PK/72 is Remel, Inc..
What is the Primary UDI-DI identifier for MICROTEST M5 (3 ML) PK/72?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00848838018350.
What classification code is assigned to this device?
This device is registered under product classification code W0104010203.
Similar Classification Devices (W0104010203)
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