Identity
- Trade Name
- CORE DYNAMICS FDA UDI
- Generic Name
- Rigid endoscopic cannula, reusable FDA UDI
- Device Name
- 5mm x 32cm Cannula with Holes, Reusable FDA UDI
- Model / Reference
- CD860 FDA UDI
- Description
- 5mm x 32cm Cannula with Holes, Reusable FDA UDI
Identifiers
- Catalog Number
- CD860 FDA UDI
- Primary DI / UDI-DI
- 20653405046360 FDA UDI
- FDA Product Code
- GCJ FDA UDI
- GMDN Term
- Rigid endoscopic cannula, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.1500 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Outer Diameter — 10 Millimeter FDA UDILength — 32 Centimeter FDA UDI
Category: Rigid endoscopic cannula, reusable
Core Dynamics by Conmed Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Rigid endoscopic cannula, reusable.
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- ECTRA — Smith & Nephew, Inc. · Class I
- Inflow cannula — SOPRO-COMEG GmbH · Class II
- Intellijet — Smith & Nephew, Inc. · Class I
- INTELIJET — Smith & Nephew, Inc. · Class I
- Intellijet — Smith & Nephew, Inc. · Class I
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Conmed Corporation
Sources (1)
- FDA UDI 90c91964-2e18-41e6-b7bb-c2c5c045f7e4 36 fields · synced May 30, 2026