eudamed_udi
Primary ID: 07330945766734
TOEOFF FLOW 2½ W/O D-RING (UDI 07330945766734)
Manufactured by Camp Scandinavia AB
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for TOEOFF FLOW 2½ W/O D-RING - Primary ID 07330945766734
Device Regulatory Overview
The TOEOFF FLOW 2½ W/O D-RING (Model/Catalog Number: 289601013) is a medical device manufactured by Camp Scandinavia AB. This product is indexed under FDA Product Code / Category Classification Y06120602 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 289601013
- Product Code / EMDN
- Y06120602
- Device Name
- TOEOFF FLOW 2½ W/O D-RING
- Database Sync Date
- 2026-08-09 16:28:47
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 TOEOFF FLOW 2½ W/O D-RING?
The registered manufacturer of record for TOEOFF FLOW 2½ W/O D-RING is Camp Scandinavia AB.
What is the Primary UDI-DI identifier for TOEOFF FLOW 2½ W/O D-RING?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07330945766734.
What classification code is assigned to this device?
This device is registered under product classification code Y06120602.
Similar Classification Devices (Y06120602)
Other Devices by Camp Scandinavia AB
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