gudid
Primary ID: Micro toothed forceps
Ambler Surgical (UDI Micro toothed 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 Micro toothed forceps
Device Regulatory Overview
The Ambler Surgical (Model/Catalog Number: Micro toothed forceps) is a medical device manufactured by AMBLER SURGICAL CORP.. This product is indexed under FDA Product Code / Category Classification GEN within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Micro toothed forceps
- Product Code / EMDN
- GEN
- Device Name
- Micro toothed forceps, 2 7/8'', straight shafts with 0.063mm 1x2 teeth set at 60 degrees, 4mm tying platforms, flat knurled handle
- Database Sync Date
- 2026-08-09 09:01:44
Full Regulatory Attributes
🔒 Token Gated
{
"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 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 Micro toothed forceps.
What classification code is assigned to this device?
This device is registered under product classification code GEN.
Similar Classification Devices (GEN)
Other Devices by AMBLER SURGICAL CORP.
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