gudid
Primary ID: RSP4
ROOT CANAL SEALER (UDI RSP4)
Manufactured by PULPDENT CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ROOT CANAL SEALER - Primary ID RSP4
Device Regulatory Overview
The ROOT CANAL SEALER (Model/Catalog Number: RSP4) is a medical device manufactured by PULPDENT CORPORATION. This product is indexed under FDA Product Code / Category Classification KIF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- RSP4
- Product Code / EMDN
- KIF
- Device Name
- Powder, 4 oz (114 gm)
- Database Sync Date
- 2026-08-09 09:03:00
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 ROOT CANAL SEALER?
The registered manufacturer of record for ROOT CANAL SEALER is PULPDENT CORPORATION.
What is the Primary UDI-DI identifier for ROOT CANAL SEALER?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is RSP4.
What classification code is assigned to this device?
This device is registered under product classification code KIF.
Similar Classification Devices (KIF)
Other Devices by PULPDENT CORPORATION
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