gudid
Primary ID: B600F
Hahnenkratt (UDI B600F)
Manufactured by E. Hahnenkratt GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Hahnenkratt - Primary ID B600F
Device Regulatory Overview
The Hahnenkratt (Model/Catalog Number: B600F) is a medical device manufactured by E. Hahnenkratt GmbH. This product is indexed under FDA Product Code / Category Classification EKB within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- B600F
- Product Code / EMDN
- EKB
- Device Name
- BLACKline ERGOtouch ExplorersForm F with handle stainless steel + DLC
- Database Sync Date
- 2026-08-09 09:07:38
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 Hahnenkratt?
The registered manufacturer of record for Hahnenkratt is E. Hahnenkratt GmbH.
What is the Primary UDI-DI identifier for Hahnenkratt?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is B600F.
What classification code is assigned to this device?
This device is registered under product classification code EKB.
Similar Classification Devices (EKB)
Other Devices by E. Hahnenkratt GmbH
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