Identity
- Trade Name
- LAP-BAND FDA UDI
- Generic Name
- Gastric band repair kit FDA UDI
- Device Name
- LAP-BAND System Tubing Kit FDA UDI
- Model / Reference
- B-20401 FDA UDI
- Description
- LAP-BAND System Tubing Kit FDA UDI
Identifiers
- Catalog Number
- B-20401 FDA UDI
- Primary DI / UDI-DI
- 10811955020503 FDA UDI
- FDA Product Code
- LTI FDA UDI
- GMDN Term
- Gastric band repair 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
No
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
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Lap-Band 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Apollo Endosurgery
Sources (1)
- FDA UDI f339f4c8-0ea1-4a10-a4d9-f6f7576fdbde 36 fields · synced Jun 8, 2026