Identity
- Trade Name
- DETACHAPORT FDA UDI
- Generic Name
- Laparoscopic access cannula, reusable FDA UDI
- Device Name
- DETACHAPORT PORT SAVER, TROCAR GHOST STICK FDA UDI
- Model / Reference
- 1-7042 FDA UDI
- Description
- DETACHAPORT PORT SAVER, TROCAR GHOST STICK FDA UDI
Identifiers
- Catalog Number
- 1-7042 FDA UDI
- Primary DI / UDI-DI
- 30653405037037 FDA UDI
- 510(k) Number
- K952977 FDA UDI
- FDA Product Code
- GCJ FDA UDI
- GMDN Term
- Laparoscopic access cannula, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.1500 FDA UDI
- Commercial Distribution
- Not 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
Detachaport by Conmed Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
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 14f7a520-29b0-4df2-b76c-48e516787714 38 fields · synced Jun 1, 2026