gudid
Primary ID: CMMX-IM05
SKaffold (UDI CMMX-IM05)
Manufactured by SKELETAL KINETICS LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SKaffold - Primary ID CMMX-IM05
Device Regulatory Overview
The SKaffold (Model/Catalog Number: CMMX-IM05) is a medical device manufactured by SKELETAL KINETICS LLC. This product is indexed under FDA Product Code / Category Classification GXP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CMMX-IM05
- Product Code / EMDN
- GXP
- Device Name
- SKaffold CMF Impress Bone Void Filler Mixing and Delivery System
- Database Sync Date
- 2026-08-09 09:43:33
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 SKaffold?
The registered manufacturer of record for SKaffold is SKELETAL KINETICS LLC.
What is the Primary UDI-DI identifier for SKaffold?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is CMMX-IM05.
What classification code is assigned to this device?
This device is registered under product classification code GXP.
Similar Classification Devices (GXP)
Other Devices by SKELETAL KINETICS LLC
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint