Spitztupfer 3 cm, armiert, Röntgenkontrast, 20-fädig, á 10 Stück, steril (UDI 04054858027401)
Manufactured by Fuhrmann GmbH
Device Regulatory Overview
The Spitztupfer 3 cm, armiert, Röntgenkontrast, 20-fädig, á 10 Stück, steril (Model/Catalog Number: 35141-1) is a medical device manufactured by Fuhrmann GmbH. This product is indexed under FDA Product Code / Category Classification M020199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 35141-1
- Product Code / EMDN
- M020199
- Device Name
- Spitztupfer mit Röntgenkonstrast, steril EO
- Database Sync Date
- 2026-08-09 16:30:42
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 Spitztupfer 3 cm, armiert, Röntgenkontrast, 20-fädig, á 10 Stück, steril?
The registered manufacturer of record for Spitztupfer 3 cm, armiert, Röntgenkontrast, 20-fädig, á 10 Stück, steril is Fuhrmann GmbH.
What is the Primary UDI-DI identifier for Spitztupfer 3 cm, armiert, Röntgenkontrast, 20-fädig, á 10 Stück, steril?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04054858027401.
What classification code is assigned to this device?
This device is registered under product classification code M020199.
Similar Classification Devices (M020199)
Other Devices by Fuhrmann GmbH
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint