GUDIDData
eudamed_udi Primary ID: 04032651988198

Pursept UniSprint Wipes FD (UDI 04032651988198)

Manufactured by Schülke & Mayr GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Pursept UniSprint Wipes FD - Primary ID 04032651988198

Device Regulatory Overview

The Pursept UniSprint Wipes FD (Model/Catalog Number: 70004263) is a medical device manufactured by Schülke & Mayr GmbH. This product is indexed under FDA Product Code / Category Classification D0799 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
70004263
Product Code / EMDN
D0799
Device Name
mikrozid universal p
Database Sync Date
2026-08-09 16:49:52

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 Pursept UniSprint Wipes FD?

The registered manufacturer of record for Pursept UniSprint Wipes FD is Schülke & Mayr GmbH.

What is the Primary UDI-DI identifier for Pursept UniSprint Wipes FD?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04032651988198.

What classification code is assigned to this device?

This device is registered under product classification code D0799.

Programmatic Export

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

JSON API Endpoint