NA
- Primary DI
- 07611819830905
- Brand
- NA
- Company
- Synthes GmbH
- Model
- 05.001.081
- Catalog number
- 05001081
- Device description
- FOOT SWITCH FOR AIR PEN DRIVE
- Published
- 2016-06-30
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- false
- Single use
- false
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| HBB | MOTOR, DRILL, PNEUMATIC |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| HBB | Motor, Drill, Pneumatic | Neurology | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K093361 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 07611819830905 | Direct Marking | GS1 | 0 | |
| 10886982129017 | Primary | GS1 | 0 | |
| H679050010810 | Secondary | HIBCC | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 07611819830905 | 07611819830905 | 7611819830905 |
| 10886982129017 | 10886982129017 |
GMDN Terms#
| Term | Definition |
|---|---|
| Foot-switch, electrical | An electrically-powered pedal used by an operator of a medical device to regulate the activation and/or intensity of a parent device (e.g., electrosurgical system generator, laser, ophthalmic examination unit, dental drill/saw system control unit) to which it is connected, typically via an electrical cable. This is a reusable device. |
Sterilization Methods#
| Method |
|---|
Contacts#
| Phone | |
|---|---|
| +1(800)255-2500 | xx@xx.xx |
Regulatory Flags#
- DUNS number
- 486711679
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- false
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- false
- Expiration date on label
- false
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- false
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 10886982030054 | LCP | 02.108.412 | 02108412 | 2015-09-14 |
| 10886982033079 | VA-LCP | 02.112.049 | 02112049 | 2015-09-14 |
| 10886982042590 | LCP | 02.124.213 | 02124213 | 2015-09-14 |
| 10886982055552 | NA | 02.221.002S | 02221002S | 2015-09-14 |
| 10886982055569 | NA | 02.221.003S | 02221003S | 2015-09-14 |
| 10886982055583 | NA | 02.221.004S | 02221004S | 2015-09-14 |
| 10886982076748 | NA | 03.221.015 | 03221015 | 2016-12-31 |
| 10886982076762 | NA | 03.221.016 | 03221016 | 2016-12-31 |
| 10886982076779 | NA | 03.221.017 | 03221017 | 2016-12-31 |
| 10886982120960 | NA | 04.221.002S | 04221002S | 2015-09-14 |
| 10886982120977 | NA | 04.221.003S | 04221003S | 2015-09-14 |
| 10886982120991 | NA | 04.221.004S | 04221004S | 2015-09-14 |
| 10886982182494 | NA | 298.800.01S | 29880001S | 2015-09-14 |
| 10886982182500 | NA | 298.801.01S | 29880101S | 2015-09-14 |
| 10886982198112 | NA | 391.103 | 391103 | 2016-12-31 |
| 10886982198129 | NA | 391.104 | 391104 | 2016-12-31 |
| 10886982198136 | NA | 391.105 | 391105 | 2016-12-31 |
| 10886982198143 | NA | 391.106 | 391106 | 2016-12-31 |
| 10886982198150 | NA | 391.107 | 391107 | 2016-12-31 |
| 10886982198167 | NA | 391.108 | 391108 | 2016-12-31 |
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| 04251388960448 | VELOCITY ALPHA ™ | adeor Medical AG | HBB | 2026-03-30 |
| 04251388961001 | VELOCITY ALPHA ™ | adeor Medical AG | HBB | 2026-03-30 |
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