eudamed_udi
Primary ID: 04260248680471
Cellutec Pro (UDI 04260248680471)
Manufactured by SLEE medical GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Cellutec Pro - Primary ID 04260248680471
Device Regulatory Overview
The Cellutec Pro (Model/Catalog Number: 11000700) is a medical device manufactured by SLEE medical GmbH. This product is indexed under FDA Product Code / Category Classification W02029099 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 11000700
- Product Code / EMDN
- W02029099
- Device Name
- Cellutec Pro
- Database Sync Date
- 2026-08-09 16:50:32
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 Cellutec Pro?
The registered manufacturer of record for Cellutec Pro is SLEE medical GmbH.
What is the Primary UDI-DI identifier for Cellutec Pro?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260248680471.
What classification code is assigned to this device?
This device is registered under product classification code W02029099.
Similar Classification Devices (W02029099)
Other Devices by SLEE medical GmbH
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