eudamed_udi
Primary ID: 07350040974322
CellaVision® DM9600 (UDI 07350040974322)
Manufactured by CellaVision AB
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CellaVision® DM9600 - Primary ID 07350040974322
Device Regulatory Overview
The CellaVision® DM9600 (Model/Catalog Number: XU-10288-01) is a medical device manufactured by CellaVision AB. This product is indexed under FDA Product Code / Category Classification W02029099 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- XU-10288-01
- Product Code / EMDN
- W02029099
- Device Name
- CellaVision® DM9600
- Database Sync Date
- 2026-08-09 16:47:16
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 CellaVision® DM9600?
The registered manufacturer of record for CellaVision® DM9600 is CellaVision AB.
What is the Primary UDI-DI identifier for CellaVision® DM9600?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07350040974322.
What classification code is assigned to this device?
This device is registered under product classification code W02029099.
Similar Classification Devices (W02029099)
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