Identity
- Trade Name
- Reprocessed PassPort Button Cannula, 8mm x 2cm FDA UDI
- Generic Name
- Laparoscopic access cannula, reprocessed FDA UDI
- Model / Reference
- AR-6592-08-20 FDA UDI
Identifiers
- Primary DI / UDI-DI
- B390AR659208201 FDA UDI
- FDA Product Code
- NBH FDA UDI
- GMDN Term
- Laparoscopic access cannula, reprocessed FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.1100 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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Laparoscopic access cannula, reprocessed
Reprocessed PassPort Button Cannula, 8mm x 2cm by Suretek Medical — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 I | Pending data |
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Manufacturer
- Manufacturer
- Suretek Medical
Sources (1)
- FDA UDI f68e57eb-e390-457b-b0c6-e9176d6f154c 32 fields · synced Jun 8, 2026