gudid
Primary ID: OS265BA-1-W
NA (UDI OS265BA-1-W)
Manufactured by PANPAC MEDICAL CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NA - Primary ID OS265BA-1-W
Device Regulatory Overview
The NA (Model/Catalog Number: OS265BA-1-W) is a medical device manufactured by PANPAC MEDICAL CORPORATION. This product is indexed under FDA Product Code / Category Classification HDQ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- OS265BA-1-W
- Product Code / EMDN
- HDQ
- Device Name
- These Cervical Dilators are especially useful in locating and dilating the external OS, the cervical canal and the internal OS. They are particularly valuable instruments to be used on post-menopausal patients with cervical stenosis.
- Database Sync Date
- 2026-08-09 09:15:29
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 NA?
The registered manufacturer of record for NA is PANPAC MEDICAL CORPORATION.
What is the Primary UDI-DI identifier for NA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is OS265BA-1-W.
What classification code is assigned to this device?
This device is registered under product classification code HDQ.
Similar Classification Devices (HDQ)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint