Buffered saline solution (UDI 08594199921212)
Manufactured by VIAMAR INTERNATIONAL, s.r.o.
Device Regulatory Overview
The Buffered saline solution (Model/Catalog Number: 98237-1) is a medical device manufactured by VIAMAR INTERNATIONAL, s.r.o.. This product is indexed under FDA Product Code / Category Classification W0104010206 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 98237-1
- Product Code / EMDN
- W0104010206
- Device Name
- Pufrovaný fyziologický roztok
- Database Sync Date
- 2026-08-09 16:29:13
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 Buffered saline solution?
The registered manufacturer of record for Buffered saline solution is VIAMAR INTERNATIONAL, s.r.o..
What is the Primary UDI-DI identifier for Buffered saline solution?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08594199921212.
What classification code is assigned to this device?
This device is registered under product classification code W0104010206.
Similar Classification Devices (W0104010206)
Other Devices by VIAMAR INTERNATIONAL, s.r.o.
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