gudid
Primary ID: Weitlaner self-retaining retractor
Ambler Surgical (UDI Weitlaner self-retaining retractor)
Manufactured by AMBLER SURGICAL CORP.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Ambler Surgical - Primary ID Weitlaner self-retaining retractor
Device Regulatory Overview
The Ambler Surgical (Model/Catalog Number: Weitlaner self-retaining retractor) is a medical device manufactured by AMBLER SURGICAL CORP.. This product is indexed under FDA Product Code / Category Classification FFO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Weitlaner self-retaining retractor
- Product Code / EMDN
- FFO
- Device Name
- Weitlaner self-retaining retractor, 4 1/2'', 2x3 blunt prongs, ring handle with ratchet catch
- Database Sync Date
- 2026-08-09 09:01:43
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 Ambler Surgical?
The registered manufacturer of record for Ambler Surgical is AMBLER SURGICAL CORP..
What is the Primary UDI-DI identifier for Ambler Surgical?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Weitlaner self-retaining retractor.
What classification code is assigned to this device?
This device is registered under product classification code FFO.
Similar Classification Devices (FFO)
Other Devices by AMBLER SURGICAL CORP.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint