Primary Device ID | 10886705029198 |
NIH Device Record Key | 3d61991f-7719-4329-a781-c2190570f2fd |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 242358 |
Catalog Number | 242358 |
Company DUNS | 482661753 |
Company Name | Medos International Sàrl |
Device Count | 1 |
DM Exempt | true |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
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 |
Phone | +1(800)255-2500 |
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Phone | +1(800)255-2500 |
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Phone | +1(800)255-2500 |
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Phone | +1(800)255-2500 |
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Phone | +1(800)255-2500 |
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Phone | +1(800)255-2500 |
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Phone | +1(800)255-2500 |
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Phone | +1(800)255-2500 |
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Phone | +1(800)255-2500 |
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Phone | +1(800)255-2500 |
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Phone | +1(800)255-2500 |
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Phone | +1(800)255-2500 |
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Phone | +1(800)255-2500 |
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Phone | +1(800)255-2500 |
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Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
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Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
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Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
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Phone | +1(800)255-2500 |
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Phone | +1(800)255-2500 |
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Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10886705029198 [Primary] |
FST | LIGHT, SURGICAL, FIBEROPTIC |
FSX | Light, surgical, connector |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-02-17 |
Device Publish Date | 2022-02-09 |
10886705027316 - NA | 2024-05-30 Latarjet EXPERIENCE, Latarjet, Glenoid Drill |
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10886705032440 - GRYPHON Flex | 2024-05-27 GRYPHON Flex Knotless Anchor Fishmouth Curved Guide |
10886705032457 - GRYPHON Flex | 2024-05-27 GRYPHON Flex Knotless Anchor Fishmouth Straight Guide |
10886705032464 - GRYPHON Flex | 2024-05-27 GRYPHON Flex Knotless Anchor Obturator |
10886705032488 - GRYPHON Flex | 2024-05-27 GRYPHON Flex Knotless PEEK Anchor PEEK Anchor STRAIGHT |
10886705032501 - GRYPHON Flex | 2024-05-27 GRYPHON Flex Knotless Anchor Curved Drill [Disposable] |
10886705032518 - GRYPHON Flex | 2024-05-27 GRYPHON Flex Knotless Anchor Sawtooth Curved Guide |