eudamed_udi
Primary ID: 06975527185018
MOLEKUR (UDI 06975527185018)
Manufactured by Shanghai Coherz Technologies Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MOLEKUR - Primary ID 06975527185018
Device Regulatory Overview
The MOLEKUR (Model/Catalog Number: N/A) is a medical device manufactured by Shanghai Coherz Technologies Co., Ltd.. This product is indexed under FDA Product Code / Category Classification Q0199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- N/A
- Product Code / EMDN
- Q0199
- Device Name
- Dental Foil
- Database Sync Date
- 2026-08-09 16:28:44
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 MOLEKUR?
The registered manufacturer of record for MOLEKUR is Shanghai Coherz Technologies Co., Ltd..
What is the Primary UDI-DI identifier for MOLEKUR?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06975527185018.
What classification code is assigned to this device?
This device is registered under product classification code Q0199.
Similar Classification Devices (Q0199)
Other Devices by Shanghai Coherz Technologies Co., Ltd.
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