eudamed_udi
Primary ID: 04987458005572
DENTAL NEEDLE (UDI 04987458005572)
Manufactured by NIPRO CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for DENTAL NEEDLE - Primary ID 04987458005572
Device Regulatory Overview
The DENTAL NEEDLE (Model/Catalog Number: 7712) is a medical device manufactured by NIPRO CORPORATION. This product is indexed under FDA Product Code / Category Classification A010601 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 7712
- Product Code / EMDN
- A010601
- Device Name
- DENTAL NEEDLE
- Database Sync Date
- 2026-08-09 16:28:56
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 DENTAL NEEDLE?
The registered manufacturer of record for DENTAL NEEDLE is NIPRO CORPORATION.
What is the Primary UDI-DI identifier for DENTAL NEEDLE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04987458005572.
What classification code is assigned to this device?
This device is registered under product classification code A010601.
Similar Classification Devices (A010601)
Other Devices by NIPRO CORPORATION
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