eudamed_udi
Primary ID: 00841435121195
SKIN HOOK DOUBLE (UDI 00841435121195)
Manufactured by Tecomet,Inc
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SKIN HOOK DOUBLE - Primary ID 00841435121195
Device Regulatory Overview
The SKIN HOOK DOUBLE (Model/Catalog Number: 2344-14-000) 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
- 2344-14-000
- Product Code / EMDN
- L0915
- Device Name
- Manipulative Instruments
- Database Sync Date
- 2026-08-09 16:29:41
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 SKIN HOOK DOUBLE?
The registered manufacturer of record for SKIN HOOK DOUBLE is Tecomet,Inc.
What is the Primary UDI-DI identifier for SKIN HOOK DOUBLE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00841435121195.
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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