eudamed_udi
Primary ID: 00841435120730
MI 2-INCISION DEAVER RETRACTOR (UDI 00841435120730)
Manufactured by Tecomet,Inc
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MI 2-INCISION DEAVER RETRACTOR - Primary ID 00841435120730
Device Regulatory Overview
The MI 2-INCISION DEAVER RETRACTOR (Model/Catalog Number: 2598-07-300) is a medical device manufactured by Tecomet,Inc. This product is indexed under FDA Product Code / Category Classification L0915 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 2598-07-300
- Product Code / EMDN
- L0915
- Device Name
- Manipulative Instruments
- Database Sync Date
- 2026-08-09 16:28:47
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 MI 2-INCISION DEAVER RETRACTOR?
The registered manufacturer of record for MI 2-INCISION DEAVER RETRACTOR is Tecomet,Inc.
What is the Primary UDI-DI identifier for MI 2-INCISION DEAVER RETRACTOR?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00841435120730.
What classification code is assigned to this device?
This device is registered under product classification code L0915.
Similar Classification Devices (L0915)
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