PROBUTIN (UDI 05904335216806)
Manufactured by LABORATOIRE L'IDEAL Parisien Sp. z o.o.
Device Regulatory Overview
The PROBUTIN (Model/Catalog Number: PROBUTIN Rectal suppositories Blister pack of 10 pieces in a carton with instructions for use. Language version: English) is a medical device manufactured by LABORATOIRE L'IDEAL Parisien Sp. z o.o.. This product is indexed under FDA Product Code / Category Classification G05 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PROBUTIN Rectal suppositories Blister pack of 10 pieces in a carton with instructions for use. Language version: English
- Product Code / EMDN
- G05
- Device Name
- Rectal suppositories / Czopki doodbytnicze
- Database Sync Date
- 2026-08-09 16:29:29
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 PROBUTIN?
The registered manufacturer of record for PROBUTIN is LABORATOIRE L'IDEAL Parisien Sp. z o.o..
What is the Primary UDI-DI identifier for PROBUTIN?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05904335216806.
What classification code is assigned to this device?
This device is registered under product classification code G05.
Similar Classification Devices (G05)
Other Devices by LABORATOIRE L'IDEAL Parisien Sp. z o.o.
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