eudamed_udi
Primary ID: 00841435121058
WIRE PULLING FORCEP (UDI 00841435121058)
Manufactured by Tecomet,Inc
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for WIRE PULLING FORCEP - Primary ID 00841435121058
Device Regulatory Overview
The WIRE PULLING FORCEP (Model/Catalog Number: 2202-00-000) is a medical device manufactured by Tecomet,Inc. This product is indexed under FDA Product Code / Category Classification L091303 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 2202-00-000
- Product Code / EMDN
- L091303
- Device Name
- Forceps
- Database Sync Date
- 2026-08-09 16:47:35
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of WIRE PULLING FORCEP?
The registered manufacturer of record for WIRE PULLING FORCEP is Tecomet,Inc.
What is the Primary UDI-DI identifier for WIRE PULLING FORCEP?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00841435121058.
What classification code is assigned to this device?
This device is registered under product classification code L091303.
Similar Classification Devices (L091303)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint