AESCULAP
- Primary DI
- 04046964105296
- Brand
- AESCULAP
- Company
- Aesculap AG
- Model
- FS618SU
- Catalog number
- FS618SU
- Device description
- ORTHOPILOT CAP SINGLE-USE MARKERS
- Published
- 2017-05-23
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- true
- Single use
- true
Related Records
Contact Domains
Product Codes
| Code | Name |
|---|---|
| HAW | Neurological stereotaxic Instrument |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| HAW | Neurological Stereotaxic Instrument | Neurology | 2 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 04046964105296 | Primary | GS1 | 0 | |
| 04046964105289 | Unit of Use | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 04046964105296 | 04046964105296 | 4046964105296 |
| 04046964105289 | 04046964105289 | 4046964105289 |
GMDN Terms
| Term | Definition |
|---|---|
| Imaging lesion localization marker, external, single-use | A device placed on the surface of a patient's body during a surgical procedure to create identifying marks that can be seen on radiographic film or digital images for the localization and delineation of areas of interest (e.g., a tumour or lesion), or attached to navigated instruments used to assist in computer-assisted surgery. It is made from materials compatible with the imaging system in which it is intended to be used [e.g., magnetic resonance imaging (MRI), x-ray, nuclear medicine], or as reflective markers detected by the cameras/computer software of an image guided surgery/patient positioning system (PPS). This is a single-use device. |
Sterilization Methods
| Method |
|---|
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
- 12
- 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
- true
- 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 |
|---|---|---|---|---|
| 04038653033997 | AESCULAP | DC230R | DC230R | 2020-06-17 |
| 04038653034321 | AESCULAP | DE112R | DE112R | 2020-06-17 |
| 04038653034369 | AESCULAP | DE116R | DE116R | 2020-06-17 |
| 04038653034376 | AESCULAP | DE117R | DE117R | 2020-06-17 |
| 04038653034406 | AESCULAP | DE120R | DE120R | 2020-06-17 |
| 04038653034901 | AESCULAP | DE676R | DE676R | 2020-06-17 |
| 04046963116194 | S4 CERVICAL | FW028U | FW028U | 2020-08-24 |
| 04046963794248 | ELAN 4 | GA768 | GA768 | 2020-04-24 |
| 04046963935184 | HI-LINE XXS | GE813SU | GE813SU | 2020-04-24 |
| 04046963935191 | HI-LINE XXS | GE814SU | GE814SU | 2020-04-24 |
| 04046963966362 | ELAN 4 | GA767 | GA767 | 2020-04-24 |
| 04046964054907 | ELAN 4 | GA715R | GA715R | 2020-04-24 |
| 04046964076664 | AESCULAP | GE812SU | GE812SU | 2020-04-24 |
| 04046964526213 | ECCOS | GB068R | GB068R | 2020-04-24 |
| 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 |
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