gudid
Primary ID: 7801S
Premium Plus (UDI 7801S)
Manufactured by Premium Plus International Limited
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Premium Plus - Primary ID 7801S
Device Regulatory Overview
The Premium Plus (Model/Catalog Number: 7801S) is a medical device manufactured by Premium Plus International Limited. This product is indexed under FDA Product Code / Category Classification KMT within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 7801S
- Product Code / EMDN
- KMT
- Device Name
- Disposable fluoride trays
- Database Sync Date
- 2026-08-09 09:01:55
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 Premium Plus?
The registered manufacturer of record for Premium Plus is Premium Plus International Limited.
What is the Primary UDI-DI identifier for Premium Plus?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 7801S.
What classification code is assigned to this device?
This device is registered under product classification code KMT.
Similar Classification Devices (KMT)
Other Devices by Premium Plus International Limited
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