eudamed_udi
Primary ID: 03665224001126
135.03XL curette dbl hemingway3 xl (UDI 03665224001126)
Manufactured by Prodont-Holliger
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for 135.03XL curette dbl hemingway3 xl - Primary ID 03665224001126
Device Regulatory Overview
The 135.03XL curette dbl hemingway3 xl (Model/Catalog Number: 135.03XL) is a medical device manufactured by Prodont-Holliger. This product is indexed under FDA Product Code / Category Classification L159001 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 135.03XL
- Product Code / EMDN
- L159001
- Device Name
- curettes
- Database Sync Date
- 2026-08-09 16:28:45
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 135.03XL curette dbl hemingway3 xl?
The registered manufacturer of record for 135.03XL curette dbl hemingway3 xl is Prodont-Holliger.
What is the Primary UDI-DI identifier for 135.03XL curette dbl hemingway3 xl?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03665224001126.
What classification code is assigned to this device?
This device is registered under product classification code L159001.
Similar Classification Devices (L159001)
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