gudid
Primary ID: S200 WALL
S200 Series (Mobile, Ceiling, Dual Ceiling, Wall) (UDI S200 WALL)
Manufactured by DENTIS CO. ,LTD
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for S200 Series (Mobile, Ceiling, Dual Ceiling, Wall) - Primary ID S200 WALL
Device Regulatory Overview
The S200 Series (Mobile, Ceiling, Dual Ceiling, Wall) (Model/Catalog Number: S200 WALL) is a medical device manufactured by DENTIS CO. ,LTD. This product is indexed under FDA Product Code / Category Classification KZF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- S200 WALL
- Product Code / EMDN
- KZF
- Device Name
- AC 100-240 V, 50/60 Hz, 58-74 VA
- Database Sync Date
- 2026-08-09 09:13:00
Full Regulatory Attributes
🔒 Token Gated
{
"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 S200 Series (Mobile, Ceiling, Dual Ceiling, Wall)?
The registered manufacturer of record for S200 Series (Mobile, Ceiling, Dual Ceiling, Wall) is DENTIS CO. ,LTD.
What is the Primary UDI-DI identifier for S200 Series (Mobile, Ceiling, Dual Ceiling, Wall)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is S200 WALL.
What classification code is assigned to this device?
This device is registered under product classification code KZF.
Similar Classification Devices (KZF)
Other Devices by DENTIS CO. ,LTD
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