eudamed_udi
Primary ID: 06945868609184
11.100.318 (UDI 06945868609184)
Manufactured by SONOSCAPE MEDICAL CORP.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for 11.100.318 - Primary ID 06945868609184
Device Regulatory Overview
The 11.100.318 (Model/Catalog Number: -) is a medical device manufactured by SONOSCAPE MEDICAL CORP.. This product is indexed under FDA Product Code / Category Classification Z12029085 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- -
- Product Code / EMDN
- Z12029085
- Device Name
- Reusable Insufflation Tubing Set
- Database Sync Date
- 2026-08-09 16:49:23
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 11.100.318?
The registered manufacturer of record for 11.100.318 is SONOSCAPE MEDICAL CORP..
What is the Primary UDI-DI identifier for 11.100.318?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06945868609184.
What classification code is assigned to this device?
This device is registered under product classification code Z12029085.
Similar Classification Devices (Z12029085)
Other Devices by SONOSCAPE MEDICAL CORP.
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