eudamed_udi
Primary ID: 03597610581281
SURFA SAFE PREMIUM (UDI 03597610581281)
Manufactured by Laboratoires Anios
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SURFA SAFE PREMIUM - Primary ID 03597610581281
Device Regulatory Overview
The SURFA SAFE PREMIUM (Model/Catalog Number: 2419544TB) is a medical device manufactured by Laboratoires Anios. This product is indexed under FDA Product Code / Category Classification D0901 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 2419544TB
- Product Code / EMDN
- D0901
- Device Name
- SURFA SAFE PREMIUM 12X750ML
- Database Sync Date
- 2026-08-09 16:29:14
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 SURFA SAFE PREMIUM?
The registered manufacturer of record for SURFA SAFE PREMIUM is Laboratoires Anios.
What is the Primary UDI-DI identifier for SURFA SAFE PREMIUM?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03597610581281.
What classification code is assigned to this device?
This device is registered under product classification code D0901.
Similar Classification Devices (D0901)
Other Devices by Laboratoires Anios
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