gudid
Primary ID: 250-259-018
RZ Medizintechnik GmbH (UDI 250-259-018)
Manufactured by RZ-Medizintechnik GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for RZ Medizintechnik GmbH - Primary ID 250-259-018
Device Regulatory Overview
The RZ Medizintechnik GmbH (Model/Catalog Number: 250-259-018) is a medical device manufactured by RZ-Medizintechnik GmbH. This product is indexed under FDA Product Code / Category Classification LRY within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 250-259-018
- Product Code / EMDN
- LRY
- Device Name
- Vertebral Distractor Spine 18mm spreading width 127mm depth
- Database Sync Date
- 2026-08-09 09:11:23
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 RZ Medizintechnik GmbH?
The registered manufacturer of record for RZ Medizintechnik GmbH is RZ-Medizintechnik GmbH.
What is the Primary UDI-DI identifier for RZ Medizintechnik GmbH?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 250-259-018.
What classification code is assigned to this device?
This device is registered under product classification code LRY.
Similar Classification Devices (LRY)
Other Devices by RZ-Medizintechnik GmbH
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint