PowerPro
- Primary DI
- 10845854018507
- Brand
- PowerPro
- Company
- Conmed Corporation
- Model
- PRO6042
- Catalog number
- PRO6042
- Device description
- POWERPRO 5:1 HIGH TORQUE CHUCK ATTACHMENT, 1/4 IN.
- Published
- 2020-09-24
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| FSM | TRAY, SURGICAL, INSTRUMENT |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| FSM | Tray, Surgical, Instrument | General, Plastic Surgery | 1 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 20845854018504 | Direct Marking | GS1 | 0 | |
| 10845854018507 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized |
|---|---|
| 20845854018504 | 20845854018504 |
| 10845854018507 | 10845854018507 |
GMDN Terms#
| Term | Definition |
|---|---|
| Reaming power tool attachment | A small component of a powered reaming assembly intended to connect to a surgical power tool system motor [it is locked and held in a collet or quick coupling and not simply gripped in a drill chuck (Jacobs chuck)] to convert the non-dedicated mechanical energy provided by the motor to a dedicated mechanical motion to perform a reaming function when an appropriate reamer endpiece (not included) is inserted. This is a reusable device. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Outer Diameter | 0.25 | Inch |
Storage And Handling#
| Type | Low | High | Condition |
|---|---|---|---|
| Special Storage Condition, Specify | 0 | 0 | KEEP DRY |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts#
| Phone | |
|---|---|
| +1(866)426-6633 | CustomerExperience@conmed.com |
Regulatory Flags#
- DUNS number
- 071595540
- Device count
- 1
- Premarket exempt
- true
- Serial number
- true
- Manufacturing date on label
- true
- Sterilization required before use
- true
Other Devices From This Company#
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|---|---|---|---|---|
| 20845854082482 | Paradigm | PEZS01A | PEZS01A | 2020-11-16 |
| 20845854015466 | SEQUENT | MR007C | MR007C | 2015-10-24 |
| 20845854036584 | SEQUENT | MR004C | MR004C | 2015-10-24 |
| 10653405044703 | CORE DYNAMICS | CD1406 | CD1406 | 2026-03-23 |
| 10653405045083 | CORE DYNAMICS | CD1608FH | CD1608FH | 2026-03-24 |
| 20653405990908 | GENESYS™ CrossFT™ | CFBC-4502R | CFBC-4502R | 2026-07-31 |
| 20653405990915 | GENESYS™ CrossFT™ | CFBC-4503R | CFBC-4503R | 2026-07-31 |
| 20653405990922 | GENESYS™ CrossFT™ | CFBC-5502R | CFBC-5502R | 2026-07-31 |
| 20653405990939 | GENESYS™ CrossFT™ | CFBC-5503R | CFBC-5503R | 2026-07-31 |
| 20653405990946 | GENESYS™ CrossFT™ | CFBC-6502R | CFBC-6502R | 2026-07-31 |
| 20653405990953 | GENESYS™ CrossFT™ | CFBC-6503R | CFBC-6503R | 2026-07-31 |
| 10653405000242 | YANKAUER | 0034470 | 0034470 | 2016-09-24 |
| 10845854035559 | E9000 | E9015 | E9015 | 2026-03-24 |
| 20653405008559 | CONMED | 60-0824-001 | 60-0824-001 | 2016-09-24 |
| 30653405003230 | CONMED | 138011 | 138011 | 2016-09-24 |
| 30653405003247 | CONMED | 138012 | 138012 | 2016-09-24 |
| 30653405058230 | AER DEFENSE | 60-8084-001 | 60-8084-001 | 2016-09-24 |
| 30845854655492 | PlumeSafe® X5™ | PX5-1354-22 | PX5-1354-22 | 2026-07-23 |
| 20845854042004 | Y-KNOT | YH01 | YH01 | 2015-10-24 |
| 20845854042028 | Y-KNOT | YH02 | YH02 | 2015-10-24 |
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| 08800037575180 | ANAX™ 5.5 SPINAL SYSTEM | CG MedTech Co.,Ltd. | FSM | 2026-09-04 |
| 08800037585110 | ANAX™ 5.5 SPINAL SYSTEM | CG MedTech Co.,Ltd. | FSM | 2026-09-04 |
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