eudamed_udi
Primary ID: G155110220
Weltianer Retractors 13 cm Blunt (UDI G155110220)
Manufactured by Nadir & CO
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Weltianer Retractors 13 cm Blunt - Primary ID G155110220
Device Regulatory Overview
The Weltianer Retractors 13 cm Blunt (Model/Catalog Number: 11022) is a medical device manufactured by Nadir & CO. This product is indexed under FDA Product Code / Category Classification L150201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 11022
- Product Code / EMDN
- L150201
- Device Name
- Weltianer Retractors 13 cm Blunt
- Database Sync Date
- 2026-08-09 16:47:33
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 Weltianer Retractors 13 cm Blunt?
The registered manufacturer of record for Weltianer Retractors 13 cm Blunt is Nadir & CO.
What is the Primary UDI-DI identifier for Weltianer Retractors 13 cm Blunt?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is G155110220.
What classification code is assigned to this device?
This device is registered under product classification code L150201.
Similar Classification Devices (L150201)
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