gudid
Primary ID: Utrata MICS capsulorhexis forceps
Ambler Surgical (UDI Utrata MICS capsulorhexis 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 Utrata MICS capsulorhexis forceps
Device Regulatory Overview
The Ambler Surgical (Model/Catalog Number: Utrata MICS capsulorhexis forceps) is a medical device manufactured by AMBLER SURGICAL CORP.. This product is indexed under FDA Product Code / Category Classification HNR within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Utrata MICS capsulorhexis forceps
- Product Code / EMDN
- HNR
- Device Name
- Utrata MICS capsulorhexis forceps, 3 1/4'', angled shafts, 12.0mm from bend to tip, delicate, serrated grasping tips, 1.8mm maximum tip spread, flat handle
- Database Sync Date
- 2026-08-09 09:01:43
Full Regulatory Attributes
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{
"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 Utrata MICS capsulorhexis forceps.
What classification code is assigned to this device?
This device is registered under product classification code HNR.
Similar Classification Devices (HNR)
Other Devices by AMBLER SURGICAL CORP.
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