gudid
Primary ID: 4517
SCHWERT (UDI 4517)
Manufactured by A. Schweickhardt GmbH & Co. KG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SCHWERT - Primary ID 4517
Device Regulatory Overview
The SCHWERT (Model/Catalog Number: 4517) is a medical device manufactured by A. Schweickhardt GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification EIK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 4517
- Product Code / EMDN
- EIK
- Device Name
- Wax knives metal, 17 cm FAHNENSTOCK, stainless
- Database Sync Date
- 2026-08-09 09:23:55
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 SCHWERT?
The registered manufacturer of record for SCHWERT is A. Schweickhardt GmbH & Co. KG.
What is the Primary UDI-DI identifier for SCHWERT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 4517.
What classification code is assigned to this device?
This device is registered under product classification code EIK.
Similar Classification Devices (EIK)
Other Devices by A. Schweickhardt GmbH & Co. KG
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