gudid
Primary ID: 29583
EXEL Dermal Curette (UDI 29583)
Manufactured by Exel International
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for EXEL Dermal Curette - Primary ID 29583
Device Regulatory Overview
The EXEL Dermal Curette (Model/Catalog Number: 29583) is a medical device manufactured by Exel International. This product is indexed under FDA Product Code / Category Classification FZS within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 29583
- Product Code / EMDN
- FZS
- Device Name
- SS, 5.0MM 50PC/BX, 6BX/CS
- Database Sync Date
- 2026-08-09 09:00:33
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 EXEL Dermal Curette?
The registered manufacturer of record for EXEL Dermal Curette is Exel International.
What is the Primary UDI-DI identifier for EXEL Dermal Curette?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 29583.
What classification code is assigned to this device?
This device is registered under product classification code FZS.
Similar Classification Devices (FZS)
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