gudid
Primary ID: 21300050
Perfectim Putty Type Kit (UDI 21300050)
Manufactured by J. MORITA U.S.A., INC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Perfectim Putty Type Kit - Primary ID 21300050
Device Regulatory Overview
The Perfectim Putty Type Kit (Model/Catalog Number: 21300050) is a medical device manufactured by J. MORITA U.S.A., INC. This product is indexed under FDA Product Code / Category Classification ELW within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 21300050
- Product Code / EMDN
- ELW
- Device Name
- PVS Dental Impression Material
- Database Sync Date
- 2026-08-09 09:49:34
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 Perfectim Putty Type Kit?
The registered manufacturer of record for Perfectim Putty Type Kit is J. MORITA U.S.A., INC.
What is the Primary UDI-DI identifier for Perfectim Putty Type Kit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 21300050.
What classification code is assigned to this device?
This device is registered under product classification code ELW.
Similar Classification Devices (ELW)
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