Identity
- Trade Name
- SPOTLIGHT FDA UDI
- Generic Name
- Laparoscopic access cannula dilator FDA UDI
- Device Name
- SPOTLIGHT ACCESS SYSTEM F2 LARGE WASHER SECOND DILATOR FDA UDI
- Model / Reference
- 275710079 FDA UDI
- Description
- SPOTLIGHT ACCESS SYSTEM F2 LARGE WASHER SECOND DILATOR FDA UDI
Identifiers
- Catalog Number
- 275710079 FDA UDI
- Primary DI / UDI-DI
- 10705034358369 FDA UDI
- FDA Product Code
- LXH FDA UDI
- GMDN Term
- Laparoscopic access cannula dilator FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.4540 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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Spotlight by Medos International Sàrl — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Medos International Sàrl
Sources (1)
- FDA UDI 62007666-9e38-4a81-a263-dea5bcae472f 36 fields · synced May 31, 2026