gudid
Primary ID: 800-162
CUTTER (UDI 800-162)
Manufactured by Ortho Arch Company Inc
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CUTTER - Primary ID 800-162
Device Regulatory Overview
The CUTTER (Model/Catalog Number: 800-162) is a medical device manufactured by Ortho Arch Company Inc. This product is indexed under FDA Product Code / Category Classification ECP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 800-162
- Product Code / EMDN
- ECP
- Device Name
- BECK DISTAL END CUTTER - FLUSH CUT
- Database Sync Date
- 2026-08-09 09:03:33
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 CUTTER?
The registered manufacturer of record for CUTTER is Ortho Arch Company Inc.
What is the Primary UDI-DI identifier for CUTTER?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 800-162.
What classification code is assigned to this device?
This device is registered under product classification code ECP.
Similar Classification Devices (ECP)
Other Devices by Ortho Arch Company Inc
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