COLUMBUS REVISION
- Primary DI
- 04046963371197
- Brand
- COLUMBUS REVISION
- Company
- Aesculap AG
- Model
- NQ675R
- Catalog number
- NQ675R
- Device description
- COLUMBUS REV TIB.BROACH/TRIAL KEEL T5
- Published
- 2020-05-08
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- false
- Single use
- false
Related Records
Contact Domains
Product Codes
| Code | Name |
|---|---|
| HTQ | BROACH |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| HTQ | Broach | Orthopedic | 1 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 04046963371197 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 04046963371197 | 04046963371197 | 4046963371197 |
GMDN Terms
| Term | Definition |
|---|---|
| Orthopaedic prosthesis implantation instrument, reusable | A hand-held surgical instrument intended to be used during implantation of an orthopaedic prosthesis, either manually or as a computer-assisted surgery (CAS) device, to aid in the navigation/placement of the prosthesis or other instruments. It may be used for the following applications: 1) to hold/align/fix bone preparation instruments, prosthesis, or prosthesis component; 2) to provide relative position landmarks; 3) to ascertain correct spatial orientation or limb alignment; and/or 4) as an interface between prosthesis components. This is a reusable device intended to be sterilized prior to use. |
Sterilization Methods
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts
| Phone | |
|---|---|
| +1(888)229-3002 | setworld_orders@aesculap.com |
| +1(800)282-9000 | GUDID.BBMUS_Service@bbraun.com |
Regulatory Flags
- DUNS number
- 315018218
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- true
- 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
- true
Other Devices From This Company
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 04038653177035 | AESCULAP | OG963R | OG963R | 2016-09-23 |
| 04038653242962 | AESCULAP | DF262R | DF262R | 2020-06-17 |
| 04038653339563 | AESCULAP | JG901 | JG901 | 2025-03-22 |
| 04038653345038 | AESCULAP | JG910 | JG910 | 2020-05-20 |
| 04038653038244 | AESCULAP | DP511R | DP511R | 2020-06-17 |
| 04038653038251 | AESCULAP | DP512R | DP512R | 2020-06-17 |
| 04038653038282 | AESCULAP | DP540R | DP540R | 2020-06-17 |
| 04038653038299 | AESCULAP | DP541R | DP541R | 2020-06-17 |
| 04038653038305 | AESCULAP | DP542R | DP542R | 2020-06-17 |
| 04038653177011 | AESCULAP | OG961R | OG961R | 2016-09-23 |
| 04038653251407 | AESCULAP | OG960R | OG960R | 2016-09-23 |
| 04038653044207 | MIASPAS MINI-ALIF | FF569R | FF569R | 2020-06-17 |
| 04038653044214 | MIASPAS MINI-ALIF | FF571R | FF571R | 2020-06-17 |
| 04038653044252 | MIASPAS MINI-ALIF | FF578R | FF578R | 2020-06-17 |
| 04038653044283 | MIASPAS MINI-ALIF | FF586R | FF586R | 2020-06-17 |
| 04038653117307 | AESCULAP | NH196 | NH196 | 2017-01-27 |
| 04038653117352 | AESCULAP | NH206 | NH206 | 2017-01-27 |
| 04038653118540 | AESCULAP | NK088 | NK088 | 2015-11-11 |
| 04038653118557 | AESCULAP | NK089 | NK089 | 2015-09-24 |
| 04038653118564 | AESCULAP | NK090 | NK090 | 2015-09-24 |
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| 00822409130979 | N/A | Ortho Development Corporation | HTQ | 2025-06-25 |
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