MOLLI
GUDID 00850024195141
MOLLI 2 Wand
Molli Surgical Inc
Imaging lesion localization marker, implantable Imaging lesion localization marker, implantable Imaging lesion localization marker, implantable Imaging lesion localization marker, implantable Imaging lesion localization marker, implantable Imaging lesion localization marker, implantable Imaging lesion localization marker, implantable Imaging lesion localization marker, implantable Imaging lesion localization marker, implantable Imaging lesion localization marker, implantable Imaging lesion localization marker, implantable Imaging lesion localization marker, implantable Imaging lesion localization marker, implantable Imaging lesion localization marker, implantable Imaging lesion localization marker, implantable Imaging lesion localization marker, implantable Imaging lesion localization marker, implantable Imaging lesion localization marker, implantable Radiological image marker, implantable Radiological image marker, implantable Radiological image marker, implantable Radiological image marker, implantable Radiological image marker, implantable Radiological image marker, implantable Radiological image marker, implantable Radiological image marker, implantable Radiological image marker, implantable Radiological image marker, implantable Radiological image marker, implantable Radiological image marker, implantable Radiological image marker, implantable| Primary Device ID | 00850024195141 |
| NIH Device Record Key | 54060090-eb34-4af4-a7fd-a8f15cfd8970 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MOLLI |
| Version Model Number | MP2001 |
| Company DUNS | 204044952 |
| Company Name | Molli Surgical Inc |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Unsafe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | true |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00850024195141 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K223107
FDA Product Code
| NEU | Marker, Radiographic, Implantable |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00850024195141]
Ethylene Oxide;Hydrogen Peroxide
[00850024195141]
Ethylene Oxide;Hydrogen Peroxide
[00850024195141]
Ethylene Oxide;Hydrogen Peroxide
[00850024195141]
Ethylene Oxide;Hydrogen Peroxide
[00850024195141]
Ethylene Oxide;Hydrogen Peroxide
[00850024195141]
Ethylene Oxide;Hydrogen Peroxide
[00850024195141]
Ethylene Oxide;Hydrogen Peroxide
[00850024195141]
Ethylene Oxide;Hydrogen Peroxide
[00850024195141]
Ethylene Oxide;Hydrogen Peroxide
[00850024195141]
Ethylene Oxide;Hydrogen Peroxide
[00850024195141]
Ethylene Oxide;Hydrogen Peroxide
[00850024195141]
Ethylene Oxide;Hydrogen Peroxide
[00850024195141]
Ethylene Oxide;Hydrogen Peroxide
[00850024195141]
Ethylene Oxide;Hydrogen Peroxide
[00850024195141]
Ethylene Oxide;Hydrogen Peroxide
[00850024195141]
Ethylene Oxide;Hydrogen Peroxide
[00850024195141]
Ethylene Oxide;Hydrogen Peroxide
[00850024195141]
Ethylene Oxide;Hydrogen Peroxide
[00850024195141]
Ethylene Oxide;Hydrogen Peroxide
[00850024195141]
Ethylene Oxide;Hydrogen Peroxide
[00850024195141]
Ethylene Oxide;Hydrogen Peroxide
[00850024195141]
Ethylene Oxide;Hydrogen Peroxide
[00850024195141]
Ethylene Oxide;Hydrogen Peroxide
[00850024195141]
Ethylene Oxide;Hydrogen Peroxide
[00850024195141]
Ethylene Oxide;Hydrogen Peroxide
[00850024195141]
Ethylene Oxide;Hydrogen Peroxide
[00850024195141]
Ethylene Oxide;Hydrogen Peroxide
[00850024195141]
Ethylene Oxide;Hydrogen Peroxide
[00850024195141]
Ethylene Oxide;Hydrogen Peroxide
[00850024195141]
Ethylene Oxide;Hydrogen Peroxide
[00850024195141]
Ethylene Oxide;Hydrogen Peroxide
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-04-07 |
| Device Publish Date | 2023-03-30 |
On-Brand Devices [MOLLI]
| 00850024195035 | MOLLI Introducer & MOLLI Marker (8 cm, 14GA) For use with the MOLLI System Note, the Introducer |
| 00850024195011 | MOLLI Tablet |
| 00850024195004 | MOLLI Wand |
| 00850024195080 | MOLLI Introducer and MOLLI Marker (12 cm, 14GA) For use with the MOLLI System Note, the Introduc |
| 00850024195165 | MOLLI re.markable (w/ 12cm Introducer) Single Unit |
| 00850024195158 | MOLLI 2 Tablet |
| 00850024195141 | MOLLI 2 Wand |
| 00850024195172 | MOLLI Pole Clamp |
| 00850024195219 | MOLLI OncoPen |
Trademark Results [MOLLI]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 MOLLI 88423318 5919596 Live/Registered |
Mediacom Communications Corporation 2019-05-09 |
 MOLLI 88423302 5919595 Live/Registered |
Mediacom Communications Corporation 2019-05-09 |
 MOLLI 88423284 5919593 Live/Registered |
Mediacom Communications Corporation 2019-05-09 |
 MOLLI 88251000 not registered Live/Pending |
MOLLI Surgical Inc. 2019-01-05 |
 MOLLI 87629387 not registered Live/Pending |
Kualli Foods, Inc 2017-09-30 |
 MOLLI 85833762 not registered Dead/Abandoned |
Kualli Foods LLC 2013-01-28 |
 MOLLI 79372664 not registered Live/Pending |
MOLLI 1886 S.A. 2023-06-01 |
 MOLLI 79192586 not registered Dead/Abandoned |
MOLLI 1886 S.A. 2016-05-27 |
 MOLLI 79115902 not registered Dead/Abandoned |
Molli 1886 SA 2012-06-14 |
 MOLLI 78961152 3396512 Dead/Cancelled |
Mazur, Robert 2006-08-26 |
 MOLLI 71417388 0372368 Dead/Cancelled |
Ruegger & Co. 1939-03-22 |
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