gudid
Primary ID: Ristow osteotome
Ambler Surgical (UDI Ristow osteotome)
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 Ristow osteotome
Device Regulatory Overview
The Ambler Surgical (Model/Catalog Number: Ristow osteotome) is a medical device manufactured by AMBLER SURGICAL CORP.. This product is indexed under FDA Product Code / Category Classification HWM within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Ristow osteotome
- Product Code / EMDN
- HWM
- Device Name
- Ristow osteotome, 8'' curved left, 5.0mm wide, single guarded cutting edge, flat handle
- Database Sync Date
- 2026-08-09 09:01:47
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 Ristow osteotome.
What classification code is assigned to this device?
This device is registered under product classification code HWM.
Similar Classification Devices (HWM)
Other Devices by AMBLER SURGICAL CORP.
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