LaparoLight LLVN12012
GUDID 30845854061347
LaparoLight Veress Needle
Conmed Corporation
Spring-loaded pneumoperitoneum needle, single-use| Primary Device ID | 30845854061347 |
| NIH Device Record Key | 92faf114-875e-4334-b859-97033028935b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | LaparoLight |
| Version Model Number | LLVN12012 |
| Catalog Number | LLVN12012 |
| Company DUNS | 071595540 |
| Company Name | Conmed Corporation |
| Device Count | 12 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
Device Dimensions
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
Operating and Storage Conditions
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00845854061346 [Unit of Use] |
| GS1 | 20845854061340 [Primary] |
| GS1 | 30845854061347 [Package] Contains: 20845854061340 Package: Box [12 Units] In Commercial Distribution |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K171139
FDA Product Code
| HIF | Insufflator, laparoscopic |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | true |
[30845854061347]
Ethylene Oxide
[30845854061347]
Ethylene Oxide
[30845854061347]
Ethylene Oxide
[30845854061347]
Ethylene Oxide
[30845854061347]
Ethylene Oxide
[30845854061347]
Ethylene Oxide
[30845854061347]
Ethylene Oxide
[30845854061347]
Ethylene Oxide
[30845854061347]
Ethylene Oxide
[30845854061347]
Ethylene Oxide
[30845854061347]
Ethylene Oxide
[30845854061347]
Ethylene Oxide
[30845854061347]
Ethylene Oxide
[30845854061347]
Ethylene Oxide
[30845854061347]
Ethylene Oxide
[30845854061347]
Ethylene Oxide
[30845854061347]
Ethylene Oxide
[30845854061347]
Ethylene Oxide
[30845854061347]
Ethylene Oxide
[30845854061347]
Ethylene Oxide
[30845854061347]
Ethylene Oxide
[30845854061347]
Ethylene Oxide
[30845854061347]
Ethylene Oxide
[30845854061347]
Ethylene Oxide
[30845854061347]
Ethylene Oxide
[30845854061347]
Ethylene Oxide
[30845854061347]
Ethylene Oxide
[30845854061347]
Ethylene Oxide
[30845854061347]
Ethylene Oxide
[30845854061347]
Ethylene Oxide
[30845854061347]
Ethylene Oxide
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-12-15 |
| Device Publish Date | 2020-12-07 |
On-Brand Devices [LaparoLight]
| 30845854061361 | LaparoLight Veress Needle |
| 30845854061347 | LaparoLight Veress Needle |
Trademark Results [LaparoLight]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 LAPAROLIGHT 88196839 5781186 Live/Registered |
Buffalo Filter LLC 2018-11-16 |
 LAPAROLIGHT 87054626 not registered Dead/Abandoned |
Buffalo Filter LLC 2016-05-31 |
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