eudamed_udi
Primary ID: 05060417200429
Gruber Specula Size 1 PK 100 (UDI 05060417200429)
Manufactured by Sheffmed Limited
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Gruber Specula Size 1 PK 100 - Primary ID 05060417200429
Device Regulatory Overview
The Gruber Specula Size 1 PK 100 (Model/Catalog Number: P60-420) is a medical device manufactured by Sheffmed Limited. This product is indexed under FDA Product Code / Category Classification Q030499 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- P60-420
- Product Code / EMDN
- Q030499
- Device Name
- Retractors - Non-Sterile
- Database Sync Date
- 2026-08-09 17:15:11
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 Gruber Specula Size 1 PK 100?
The registered manufacturer of record for Gruber Specula Size 1 PK 100 is Sheffmed Limited.
What is the Primary UDI-DI identifier for Gruber Specula Size 1 PK 100?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05060417200429.
What classification code is assigned to this device?
This device is registered under product classification code Q030499.
Similar Classification Devices (Q030499)
Other Devices by Sheffmed Limited
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