Identity
- Trade Name
- Access Port RapidPort EZ Kit FDA UDI
- Generic Name
- Gastric band access port kit FDA UDI
- Device Name
- RAPIDPORT EZ Access Port Kit 10CC FDA UDI
- Model / Reference
- B-2304 FDA UDI
- Description
- RAPIDPORT EZ Access Port Kit 10CC FDA UDI
Identifiers
- Catalog Number
- B-2304 FDA UDI
- Primary DI / UDI-DI
- 10811955020244 FDA UDI
- FDA Product Code
- LTI FDA UDI
- GMDN Term
- Gastric band access port kit FDA UDI
Classification
- Device Class
- Class III FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
MR Conditional FDA UDI
Access Port RapidPort EZ Kit by Apollo Endosurgery — Class III — 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 III | Pending data |
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Manufacturer
- Manufacturer
- Apollo Endosurgery
Sources (1)
- FDA UDI cc8db587-0403-42c3-aa96-0496afacac38 37 fields · synced May 30, 2026