PROTEOSE PEPTONE (PROTEOSE PEPTONE) (UDI 05940540373224)
Manufactured by Sanimed International Impex S.A.
Device Regulatory Overview
The PROTEOSE PEPTONE (PROTEOSE PEPTONE) (Model/Catalog Number: 41935) is a medical device manufactured by Sanimed International Impex S.A.. This product is indexed under FDA Product Code / Category Classification W0104010101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 41935
- Product Code / EMDN
- W0104010101
- Device Name
- PROTEOSE PEPTONE (PROTEOSE PEPTONE)
- Database Sync Date
- 2026-08-09 16:50:29
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 PROTEOSE PEPTONE (PROTEOSE PEPTONE)?
The registered manufacturer of record for PROTEOSE PEPTONE (PROTEOSE PEPTONE) is Sanimed International Impex S.A..
What is the Primary UDI-DI identifier for PROTEOSE PEPTONE (PROTEOSE PEPTONE)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05940540373224.
What classification code is assigned to this device?
This device is registered under product classification code W0104010101.
Similar Classification Devices (W0104010101)
Other Devices by Sanimed International Impex S.A.
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