Primary Device ID | 10886705029228 |
NIH Device Record Key | 48ee34eb-d41f-47db-bd80-7112e61cc774 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 242361 |
Catalog Number | 242361 |
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 |
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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 |
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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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10886705029228 [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 |
10886705001507 - GRYPHON | 2025-03-18 GRYPHON OBTURATOR |
10886705001538 - GRYPHON | 2025-03-18 GRYPHON BLUNT OBTURATOR |
10886705002634 - RIGIDFIX | 2025-03-18 RIGIDFIX Femoral/Tibial Rod Thumb Screw |
10886705002993 - RIGIDFIX | 2025-03-18 RIGIDFIX Mallet |
10886705003440 - NA | 2025-03-18 REUSABLE OBTURATOR 5.5 x 55mm |
10886705003464 - NA | 2025-03-18 REUSABLE OBTURATOR 5.5 x 75mm |
10886705003501 - NA | 2025-03-18 REUSABLE OBTURATOR 5.5 x 90mm |
10886705003525 - NA | 2025-03-18 REUSABLE OBTURATOR 7.0 x 110mm |