eudamed_udi
Primary ID: 05060417200375
Tumarkin Specula Size 3 PK 100 (UDI 05060417200375)
Manufactured by Sheffmed Limited
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Tumarkin Specula Size 3 PK 100 - Primary ID 05060417200375
Device Regulatory Overview
The Tumarkin Specula Size 3 PK 100 (Model/Catalog Number: P60-403) 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
- P60-403
- Product Code / EMDN
- Q030499
- Device Name
- Retractors - Non-Sterile
- Database Sync Date
- 2026-08-09 16:29:13
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 Tumarkin Specula Size 3 PK 100?
The registered manufacturer of record for Tumarkin Specula Size 3 PK 100 is Sheffmed Limited.
What is the Primary UDI-DI identifier for Tumarkin Specula Size 3 PK 100?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05060417200375.
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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