eudamed_udi
Primary ID: 04251992197896
JOSI-Ultra Rückensystem RS 2, RH 50 cm (UDI 04251992197896)
Manufactured by John GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for JOSI-Ultra Rückensystem RS 2, RH 50 cm - Primary ID 04251992197896
Device Regulatory Overview
The JOSI-Ultra Rückensystem RS 2, RH 50 cm (Model/Catalog Number: GURT-30000-M-37-6) is a medical device manufactured by John GmbH. This product is indexed under FDA Product Code / Category Classification Y180999 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- GURT-30000-M-37-6
- Product Code / EMDN
- Y180999
- Device Name
- Rollstuhlzubehör
- Database Sync Date
- 2026-08-09 16:47:12
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of JOSI-Ultra Rückensystem RS 2, RH 50 cm?
The registered manufacturer of record for JOSI-Ultra Rückensystem RS 2, RH 50 cm is John GmbH.
What is the Primary UDI-DI identifier for JOSI-Ultra Rückensystem RS 2, RH 50 cm?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04251992197896.
What classification code is assigned to this device?
This device is registered under product classification code Y180999.
Similar Classification Devices (Y180999)
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