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Primary ID: P990033
PEPGEN P-15, PEPGEN P-15 FLOW, AND PEPGEN P-15 PUTTY (UDI P990033)
Manufactured by Ceramed Corp.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PEPGEN P-15, PEPGEN P-15 FLOW, AND PEPGEN P-15 PUTTY - Primary ID P990033
Device Regulatory Overview
The PEPGEN P-15, PEPGEN P-15 FLOW, AND PEPGEN P-15 PUTTY (Model/Catalog Number: Unspecified) is a medical device manufactured by Ceramed Corp.. This product is indexed under FDA Product Code / Category Classification NPZ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- N/A
- Product Code / EMDN
- NPZ
- Device Name
- Bone grafting material, dental, with biologic component
- Database Sync Date
- 2026-08-09 10:06:18
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 PEPGEN P-15, PEPGEN P-15 FLOW, AND PEPGEN P-15 PUTTY?
The registered manufacturer of record for PEPGEN P-15, PEPGEN P-15 FLOW, AND PEPGEN P-15 PUTTY is Ceramed Corp..
What is the Primary UDI-DI identifier for PEPGEN P-15, PEPGEN P-15 FLOW, AND PEPGEN P-15 PUTTY?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is P990033.
What classification code is assigned to this device?
This device is registered under product classification code NPZ.
Similar Classification Devices (NPZ)
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