| Primary Device ID | 18033509851728 |
| NIH Device Record Key | 4b15926b-18a4-467e-bbda-504527aba12f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Hybrid Fixator System |
| Version Model Number | 1 |
| Catalog Number | 99-80122 |
| Company DUNS | 438793622 |
| Company Name | ORTHOFIX SRL |
| Device Count | 1 |
| 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 | true |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +039456719000 |
| info@orthofix.it | |
| Phone | +039456719000 |
| info@orthofix.it | |
| Phone | +039456719000 |
| info@orthofix.it | |
| Phone | +039456719000 |
| info@orthofix.it | |
| Phone | +039456719000 |
| info@orthofix.it | |
| Phone | +039456719000 |
| info@orthofix.it | |
| Phone | +039456719000 |
| info@orthofix.it | |
| Phone | +039456719000 |
| info@orthofix.it | |
| Phone | +039456719000 |
| info@orthofix.it | |
| Phone | +039456719000 |
| info@orthofix.it | |
| Phone | +039456719000 |
| info@orthofix.it | |
| Phone | +039456719000 |
| info@orthofix.it | |
| Phone | +039456719000 |
| info@orthofix.it | |
| Phone | +039456719000 |
| info@orthofix.it | |
| Phone | +039456719000 |
| info@orthofix.it |
| Length | 400 Millimeter |
| Outer Diameter | 2 Millimeter |
| Length | 400 Millimeter |
| Outer Diameter | 2 Millimeter |
| Length | 400 Millimeter |
| Outer Diameter | 2 Millimeter |
| Length | 400 Millimeter |
| Outer Diameter | 2 Millimeter |
| Length | 400 Millimeter |
| Outer Diameter | 2 Millimeter |
| Length | 400 Millimeter |
| Outer Diameter | 2 Millimeter |
| Length | 400 Millimeter |
| Outer Diameter | 2 Millimeter |
| Length | 400 Millimeter |
| Outer Diameter | 2 Millimeter |
| Length | 400 Millimeter |
| Outer Diameter | 2 Millimeter |
| Length | 400 Millimeter |
| Outer Diameter | 2 Millimeter |
| Length | 400 Millimeter |
| Outer Diameter | 2 Millimeter |
| Length | 400 Millimeter |
| Outer Diameter | 2 Millimeter |
| Length | 400 Millimeter |
| Outer Diameter | 2 Millimeter |
| Length | 400 Millimeter |
| Outer Diameter | 2 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 18033509851728 [Primary] |
| JEC | Component, Traction, Invasive |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2015-09-01 |
| 18033509851766 | X-WIRE WITHOUT OLIVE STERILE DIAMETER 1,8 MM LENGTH 400 MM |
| 18033509851759 | X-WIRE WITH CENTRAL OLIVE STERILE DIAMETER 1,8 MM LENGTH 400 MM |
| 18033509851742 | X-WIRE WITHOUT OLIVE STERILE DIAMETER 2 MM LENGTH 450 MM |
| 18033509851735 | X-WIRE WITH CENTRAL OLIVE STERILE DIAMETER 2 MM LENGTH 450 MM |
| 18033509851728 | X-WIRE WITHOUT OLIVE STERILE DIAMETER 2 MM LENGTH 400 MM |
| 18033509851711 | X-WIRE WITH CENTRAL OLIVE STERILE DIAMETER 2 MM LENGTH 400 MM |
| 18033509851704 | X-WIRE WITH LATERAL OLIVE STERILE DIAMETER 2 MM LENGTH 400 MM |
| 18033509851698 | X-WIRE WITH LATERAL OLIVE STERILE DIAMETER 2 MM LENGTH 350 MM |
| 18033509851681 | X-WIRE WITH LATERAL OLIVE STERILE DIAMETER 2 MM LENGTH 310 MM |
| 18032568869217 | X-WIRE WITHOUT OLIVE DIAMETER 1,8 MM LENGTH 400 MM |
| 18032568869200 | X-WIRE WITH CENTRAL OLIVE DIAMETER 1,8 MM LENGTH 400 MM |
| 18032568860955 | HYBRID SYSTEM STERI BOX EMPTY |
| 18032568860948 | HYBRID SYSTEM STERI BOX EMPTY |
| 18032568860832 | SUPPLEMENTARY SCREW HOLDER BAR RADIOLUCENT 300 MM |
| 18032568860597 | WIRE COVERS (PACK OF 20) |
| 18032568860580 | X-WIRE WITHOUT OLIVE DIAMETER 2 MM LENGTH 450 MM |
| 18032568860573 | X-WIRE WITH CENTRAL OLIVE DIAMETER 2 MM LENGTH 450 MM |
| 18032568860566 | X-WIRE WITHOUT OLIVE DIAMETER 2 MM LENGTH 400 MM |
| 18032568860559 | X-WIRE WITH CENTRAL OLIVE DIAMETER 2 MM LENGTH 400 MM |
| 18032568860542 | X-WIRE WITH LATERAL OLIVE DIAMETER 2 MM LENGTH 400 MM |
| 18032568860535 | X-WIRE WITH LATERAL OLIVE DIAMETER 2 MM LENGTH 350 MM |
| 18032568860528 | X-WIRE WITH LATERAL OLIVE DIAMETER 2 MM LENGTH 310 MM |
| 18032568860474 | ASSEMBLY KIT SHORT FOR HYBRID PROCALLUS |
| 18032568860467 | ASSEMBLY KIT STANDARD FOR HYBRID PROCALLUS |
| 18032568860450 | HYBRID COUPLING WITH BALL-JOINT |
| 18032568860436 | POST LENGTH 150 MM |
| 18032568860412 | POST LENGTH 100 MM |
| 18032568860405 | SUPPLEMENTARY SCREW HOLDER BAR DIAMETER 6 MM LENGTH 300 MM |
| 18032568860399 | POST LENGTH 50 MM |
| 18032568860382 | INDEPENDENT WIRE CLAMP |
| 18032568860290 | 3-HOLE WIRE CLAMP SLIDER UNIT |
| 18032568860276 | TWO-HOLE K-WIRE SECURING PIN |
| 18032568035193 | HYBRID COUPLING TEMPLATE WITH BALL-JOINT (10000 SERIES) |
| 18032568035186 | WIRE GUIDE |
| 18032568035179 | WIRE TENSIONER |
| 18053504366188 | Spare part, not medical device, not for sale. Reported for registration of UDI direct marking. |
| 18053504365778 | Component. Not for sale. Used for reporting Direct Marking of assembly. |