eudamed_udi
Primary ID: 07340194302836
Proctoscope Select™ (UDI 07340194302836)
Manufactured by Cetro Medical AB
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Proctoscope Select™ - Primary ID 07340194302836
Device Regulatory Overview
The Proctoscope Select™ (Model/Catalog Number: 1541) is a medical device manufactured by Cetro Medical AB. This product is indexed under FDA Product Code / Category Classification G02060302 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1541
- Product Code / EMDN
- G02060302
- Device Name
- Anal endoscopic device
- Database Sync Date
- 2026-08-09 16:44:47
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 Proctoscope Select™?
The registered manufacturer of record for Proctoscope Select™ is Cetro Medical AB.
What is the Primary UDI-DI identifier for Proctoscope Select™?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07340194302836.
What classification code is assigned to this device?
This device is registered under product classification code G02060302.
Similar Classification Devices (G02060302)
Other Devices by Cetro Medical AB
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