gudid
Primary ID: 1
Respire Pink AT Hard (UDI 1)
Manufactured by Ortho Solutions, LC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Respire Pink AT Hard - Primary ID 1
Device Regulatory Overview
The Respire Pink AT Hard (Model/Catalog Number: 1) is a medical device manufactured by Ortho Solutions, LC. This product is indexed under FDA Product Code / Category Classification LRK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1
- Product Code / EMDN
- LRK
- Device Name
- Database Sync Date
- 2026-08-09 09:03:36
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Respire Pink AT Hard?
The registered manufacturer of record for Respire Pink AT Hard is Ortho Solutions, LC.
What is the Primary UDI-DI identifier for Respire Pink AT Hard?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1.
What classification code is assigned to this device?
This device is registered under product classification code LRK.
Similar Classification Devices (LRK)
Other Devices by Ortho Solutions, LC
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint