gudid
Primary ID: 62200
NA (UDI 62200)
Manufactured by Nobel Biocare AB
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NA - Primary ID 62200
Device Regulatory Overview
The NA (Model/Catalog Number: 62200) is a medical device manufactured by Nobel Biocare AB. This product is indexed under FDA Product Code / Category Classification EGD within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 62200
- Product Code / EMDN
- EGD
- Device Name
- Abutment Scr, Slotted, 3.25HL/3.5, 4-Pk
- Database Sync Date
- 2026-08-09 09:08:31
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 NA?
The registered manufacturer of record for NA is Nobel Biocare AB.
What is the Primary UDI-DI identifier for NA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 62200.
What classification code is assigned to this device?
This device is registered under product classification code EGD.
Similar Classification Devices (EGD)
Other Devices by Nobel Biocare AB
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