eudamed_udi
Primary ID: 04066098220023
Blutabnahme- Patientenstuhl Serie 22 (UDI 04066098220023)
Manufactured by Greiner GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Blutabnahme- Patientenstuhl Serie 22 - Primary ID 04066098220023
Device Regulatory Overview
The Blutabnahme- Patientenstuhl Serie 22 (Model/Catalog Number: 2207340) is a medical device manufactured by Greiner GmbH. This product is indexed under FDA Product Code / Category Classification V080202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 2207340
- Product Code / EMDN
- V080202
- Device Name
- Blutentnahmestuhl / Patientenstuhl
- Database Sync Date
- 2026-08-09 16:29:21
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 Blutabnahme- Patientenstuhl Serie 22?
The registered manufacturer of record for Blutabnahme- Patientenstuhl Serie 22 is Greiner GmbH.
What is the Primary UDI-DI identifier for Blutabnahme- Patientenstuhl Serie 22?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04066098220023.
What classification code is assigned to this device?
This device is registered under product classification code V080202.
Similar Classification Devices (V080202)
Other Devices by Greiner GmbH
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