Identity
- Trade Name
- ANCHORPORT FDA UDI
- Generic Name
- Laparoscopic access cannula, single-use FDA UDI
- Device Name
- ANCHORPORT 5MM CANNULA WITHOUT INSUFFLATION PORT, 135MM LONG FDA UDI
- Model / Reference
- APC5-135 FDA UDI
- Description
- ANCHORPORT 5MM CANNULA WITHOUT INSUFFLATION PORT, 135MM LONG FDA UDI
Identifiers
- Catalog Number
- APC5-135 FDA UDI
- Primary DI / UDI-DI
- 10851885004518 FDA UDI
- FDA Product Code
- GCJ FDA UDI
- GMDN Term
- Laparoscopic access cannula, single-use 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
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
- Outer Diameter — 5 Millimeter FDA UDILength — 135 Millimeter FDA UDI
Anchorport by Conmed Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 1d6a3491-5f1d-48b0-ac3b-9894d02cbf88 37 fields · synced May 31, 2026