eudamed_udi
Primary ID: 07611600263011
Cellodent (UDI 07611600263011)
Manufactured by IVF HARTMANN AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Cellodent - Primary ID 07611600263011
Device Regulatory Overview
The Cellodent (Model/Catalog Number: 263010) is a medical device manufactured by IVF HARTMANN AG. This product is indexed under FDA Product Code / Category Classification M020299 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 263010
- Product Code / EMDN
- M020299
- Device Name
- Cellodent swabs
- Database Sync Date
- 2026-08-09 18:46:04
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 Cellodent?
The registered manufacturer of record for Cellodent is IVF HARTMANN AG.
What is the Primary UDI-DI identifier for Cellodent?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07611600263011.
What classification code is assigned to this device?
This device is registered under product classification code M020299.
Similar Classification Devices (M020299)
Other Devices by IVF HARTMANN AG
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