Identity
- Trade Name
- LaparoLight EUDAMEDFDA UDI
- Generic Name
- Spring-loaded pneumoperitoneum needle, single-use FDA UDI
- Device Name
- Surgical Instruments and Accessories EUDAMEDLaparoLight Veress Needle (120 mm) Laparoscopic Solutions FDA UDILaparoLight Veress Needle (150 mm) Laparoscopic Solutions FDA UDI
- Model / Reference
- LLVN15012 EUDAMEDFDA UDILLVN12012 FDA UDI
- Description
- LaparoLight Veress Needle (120 mm) Laparoscopic Solutions FDA UDILaparoLight Veress Needle (150 mm) Laparoscopic Solutions FDA UDI
Identifiers
- Catalog Number
- LLVN12012 FDA UDILLVN15012 FDA UDI
- Primary DI / UDI-DI
- 20845854061364 EUDAMEDFDA UDI20845854061340 FDA UDI
- Basic UDI-DI
- B-20845854061364 EUDAMED
- 510(k) Number
- K171139 FDA UDI
- FDA Product Code
- HIF FDA UDI
- EMDN Code
- K0104 VERESS NEEDLES EUDAMED
- GMDN Term
- Spring-loaded pneumoperitoneum needle, single-use FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass II FDA UDI
- Regulation Number
- 884.1730 FDA UDI
- Market of Registration
- Belgium EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
EUDAMEDFDA UDI
Single Use
Yes
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Ethylene Oxide FDA UDI
Category: Spring-loaded pneumoperitoneum needle, single-use
LaparoLight by Conmed Corporation — Class II — MDD, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
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Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Unknown
MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDD | — | Class II | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Conmed Corporation
Sources (3)
- FDA UDI 92faf114-875e-4334-b859-97033028935b 38 fields · synced Jul 18, 2026
- FDA UDI d760332e-909f-4b48-906c-81e2057a16c2 38 fields · synced May 30, 2026
- EUDAMED b7148f61-5008-4295-819f-dc689ed03f4a 61 fields · synced Jul 18, 2026