GUDIDData
eudamed_udi Primary ID: 04031678082674

Mikrobac Tissues (UDI 04031678082674)

Manufactured by BODE Chemie GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Mikrobac Tissues - Primary ID 04031678082674

Device Regulatory Overview

The Mikrobac Tissues (Model/Catalog Number: 981809) is a medical device manufactured by BODE Chemie GmbH. This product is indexed under FDA Product Code / Category Classification D99 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
981809
Product Code / EMDN
D99
Device Name
Mikrobac
Database Sync Date
2026-08-09 18:19:10

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 Mikrobac Tissues?

The registered manufacturer of record for Mikrobac Tissues is BODE Chemie GmbH.

What is the Primary UDI-DI identifier for Mikrobac Tissues?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04031678082674.

What classification code is assigned to this device?

This device is registered under product classification code D99.

Programmatic Export

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

JSON API Endpoint