Identity
- Trade Name
- OBALON® FDA UDI
- Generic Name
- Gastrointestinal catheter/endoscope tracking system FDA UDI
- Device Name
- OBALON® Recalibration Tool - component for use with the OBALON® Navigation Console FDA UDI
- Model / Reference
- 7405-0001 FDA UDI
- Description
- OBALON® Recalibration Tool - component for use with the OBALON® Navigation Console FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00859810006241 FDA UDI
- FDA Product Code
- LTI FDA UDI
- GMDN Term
- Gastrointestinal catheter/endoscope tracking system FDA UDI
Classification
- Device Class
- Class III 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
No
FDA UDI
MR Unsafe FDA UDI
Obalon® by ReShape Lifesciences Inc. — 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
- ReShape Lifesciences Inc.
Sources (1)
- FDA UDI 8ae27967-8db1-4964-b636-8918e039b99d 36 fields · synced Jun 8, 2026