eudamed_udi
Primary ID: 07611600997114
Patient BE (UDI 07611600997114)
Manufactured by IVF HARTMANN AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Patient BE - Primary ID 07611600997114
Device Regulatory Overview
The Patient BE (Model/Catalog Number: 990587) is a medical device manufactured by IVF HARTMANN AG. This product is indexed under FDA Product Code / Category Classification V0599 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 990587
- Product Code / EMDN
- V0599
- Device Name
- Garment Sets non-sterile
- Database Sync Date
- 2026-08-09 17:42:23
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 Patient BE?
The registered manufacturer of record for Patient BE is IVF HARTMANN AG.
What is the Primary UDI-DI identifier for Patient BE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07611600997114.
What classification code is assigned to this device?
This device is registered under product classification code V0599.
Similar Classification Devices (V0599)
Other Devices by IVF HARTMANN AG
Programmatic Export
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