gudid
Primary ID: Wies chalazion forceps
Ambler Surgical (UDI Wies chalazion forceps)
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 Wies chalazion forceps
Device Regulatory Overview
The Ambler Surgical (Model/Catalog Number: Wies chalazion forceps) is a medical device manufactured by AMBLER SURGICAL CORP.. This product is indexed under FDA Product Code / Category Classification HOD within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Wies chalazion forceps
- Product Code / EMDN
- HOD
- Device Name
- Wies chalazion forceps, 15.0mm solid lower plate, 9.0mm x 12.0mm open serrated upper plate, locking thumb screw, flat handle
- Database Sync Date
- 2026-08-09 09:01:49
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 Wies chalazion forceps.
What classification code is assigned to this device?
This device is registered under product classification code HOD.
Similar Classification Devices (HOD)
Other Devices by AMBLER SURGICAL CORP.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint