pma Primary ID: P990033

PEPGEN P-15, PEPGEN P-15 FLOW & PEPGEN P-15 PUTTY (UDI P990033)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The PEPGEN P-15, PEPGEN P-15 FLOW & 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 10:06:24

Full Regulatory Attributes

🔒 Token Gated

{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of PEPGEN P-15, PEPGEN P-15 FLOW & PEPGEN P-15 PUTTY?

The registered manufacturer of record for PEPGEN P-15, PEPGEN P-15 FLOW & PEPGEN P-15 PUTTY is Ceramed Corp..

What is the Primary UDI-DI identifier for PEPGEN P-15, PEPGEN P-15 FLOW & 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)

Other Devices by Ceramed Corp.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint