GUDIDData
gudid Primary ID: 00700

P&P Medical Surgical LLC (UDI 00700)

Manufactured by P&P Medical Surgical LLC

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for P&P Medical Surgical LLC - Primary ID 00700

Device Regulatory Overview

The P&P Medical Surgical LLC (Model/Catalog Number: 00700) is a medical device manufactured by P&P Medical Surgical LLC. This product is indexed under FDA Product Code / Category Classification KXF within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
00700
Product Code / EMDN
KXF
Device Name
Sterile Cotton Tipped Applicator 6" Box of 100
Database Sync Date
2026-08-09 09:04:05

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 P&P Medical Surgical LLC?

The registered manufacturer of record for P&P Medical Surgical LLC is P&P Medical Surgical LLC.

What is the Primary UDI-DI identifier for P&P Medical Surgical LLC?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00700.

What classification code is assigned to this device?

This device is registered under product classification code KXF.

Programmatic Export

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

JSON API Endpoint