Identity
- Trade Name
- CORE DYNAMICS FDA UDI
- Generic Name
- Laparoscopic blunt dissector FDA UDI
- Device Name
- 5mm Laparoscopic Kittner FDA UDI
- Model / Reference
- CD802 FDA UDI
- Description
- 5mm Laparoscopic Kittner FDA UDI
Identifiers
- Catalog Number
- CD802 FDA UDI
- Primary DI / UDI-DI
- 20653405043284 FDA UDI
- 510(k) Number
- K955490 FDA UDI
- FDA Product Code
- GCJ FDA UDI
- GMDN Term
- Laparoscopic blunt dissector 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
Yes
FDA UDI
Single Use
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Ethylene Oxide FDA UDI
Dimensions & Sizes
- Size
- Length — 40 Centimeter FDA UDIOuter Diameter — 5 Millimeter FDA UDI
Category: Laparoscopic blunt dissector
Core Dynamics by Conmed Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Laparoscopic blunt dissector.
- Snowden-Pencer — STERIS CORPORATION · Class II
- Flex — Medrobotics Corporation · Class II
- DeRoyal — DEROYAL INDUSTRIES, INC. · Class I
- Medline — MEDLINE INDUSTRIES, INC. · Class II
- MEDLINE — MEDLINE INDUSTRIES, INC. · U
- FLEX — Medrobotics Corporation · Class II
- Snowden-Pencer — STERIS CORPORATION · Class II
- Medline — MEDLINE INDUSTRIES, INC. · Class II
Cleared under the same submission
K955490 also covers:
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Conmed Corporation
Sources (1)
- FDA UDI 65a1dceb-85f9-4cc9-87ba-3e8281195a69 37 fields · synced Jun 8, 2026