gudid
Primary ID: 700-612
ORTHO ARCH (UDI 700-612)
Manufactured by Ortho Arch Company Inc
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ORTHO ARCH - Primary ID 700-612
Device Regulatory Overview
The ORTHO ARCH (Model/Catalog Number: 700-612) 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
- 700-612
- Product Code / EMDN
- ECP
- Device Name
- INFANT TRAINER PHASE II
- 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 ORTHO ARCH?
The registered manufacturer of record for ORTHO ARCH is Ortho Arch Company Inc.
What is the Primary UDI-DI identifier for ORTHO ARCH?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 700-612.
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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