HEATH Ligatur Schere (UDI 04250379808103)
Manufactured by Zepf Medical Instruments GmbH
Device Regulatory Overview
The HEATH Ligatur Schere (Model/Catalog Number: 08-8009-15) is a medical device manufactured by Zepf Medical Instruments GmbH. This product is indexed under FDA Product Code / Category Classification L01040299 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 08-8009-15
- Product Code / EMDN
- L01040299
- Device Name
- Schere, Wundnaht
- Database Sync Date
- 2026-08-09 17:02:59
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 HEATH Ligatur Schere?
The registered manufacturer of record for HEATH Ligatur Schere is Zepf Medical Instruments GmbH.
What is the Primary UDI-DI identifier for HEATH Ligatur Schere?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04250379808103.
What classification code is assigned to this device?
This device is registered under product classification code L01040299.
Similar Classification Devices (L01040299)
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