gudid
Primary ID: 12200003Z
ArcCHECK PMMA MultiPlug (UDI 12200003Z)
Manufactured by SUN NUCLEAR CORP.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ArcCHECK PMMA MultiPlug - Primary ID 12200003Z
Device Regulatory Overview
The ArcCHECK PMMA MultiPlug (Model/Catalog Number: 12200003Z) is a medical device manufactured by SUN NUCLEAR CORP.. This product is indexed under FDA Product Code / Category Classification LHO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 12200003Z
- Product Code / EMDN
- LHO
- Device Name
- Accessory to Models 1220 ArcCHECK and 1220-MR ArcCHECK-MR.
- Database Sync Date
- 2026-08-09 09:16:43
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 ArcCHECK PMMA MultiPlug?
The registered manufacturer of record for ArcCHECK PMMA MultiPlug is SUN NUCLEAR CORP..
What is the Primary UDI-DI identifier for ArcCHECK PMMA MultiPlug?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 12200003Z.
What classification code is assigned to this device?
This device is registered under product classification code LHO.
Similar Classification Devices (LHO)
Other Devices by SUN NUCLEAR CORP.
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