gudid
Primary ID: EBP20100-F
V. Mueller (UDI EBP20100-F)
Manufactured by CAREFUSION 2200, INC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for V. Mueller - Primary ID EBP20100-F
Device Regulatory Overview
The V. Mueller (Model/Catalog Number: EBP20100-F) is a medical device manufactured by CAREFUSION 2200, INC. This product is indexed under FDA Product Code / Category Classification GEI within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- EBP20100-F
- Product Code / EMDN
- GEI
- Device Name
- V. Mueller BAYONET BIPOLAR FORCEPS NON-STICK, TIP 1.0MM LENGTH: 8IN. (20.3CM) SINGLE USE
- Database Sync Date
- 2026-08-09 09:16:32
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 V. Mueller?
The registered manufacturer of record for V. Mueller is CAREFUSION 2200, INC.
What is the Primary UDI-DI identifier for V. Mueller?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is EBP20100-F.
What classification code is assigned to this device?
This device is registered under product classification code GEI.
Similar Classification Devices (GEI)
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