gudid
Primary ID: 926-2
SCHWERT (UDI 926-2)
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 926-2
Device Regulatory Overview
The SCHWERT (Model/Catalog Number: 926-2) is a medical device manufactured by A. Schweickhardt GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification EMM within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 926-2
- Product Code / EMDN
- EMM
- Device Name
- Chisels cvd. 13cm 2mm vienna model
- 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 926-2.
What classification code is assigned to this device?
This device is registered under product classification code EMM.
Similar Classification Devices (EMM)
Other Devices by A. Schweickhardt GmbH & Co. KG
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