PROSPACE®
- Primary DI
- 04046963806125
- Brand
- PROSPACE®
- Company
- Aesculap AG
- Model
- SN041P
- Catalog number
- SN041P
- Device description
- PROSPACE PEEK IMPLANT 5° 11X8.5X22MM
- Published
- 2015-09-24
- Public version status
- Update
- Distribution status
- Not in Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- Sterile
- true
- Single use
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| MAX | Intervertebral fusion device with bone graft, lumbar |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | Orthopedic | 2 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 04046963806125 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 04046963806125 | 04046963806125 | 4046963806125 |
GMDN Terms#
| Term | Definition |
|---|---|
| Polymeric spinal fusion cage, sterile | A sterile device intended to help fuse segments of the spine to treat anatomical abnormalities of the vertebrae, typically due to degenerative intervertebral disks [i.e., degenerative disc disease (DDD)]. The device is typically designed as a small, hollow and/or porous, threaded or fenestrated cylinder (or other geometric form) and is made of non-bioabsorbable synthetic polymer [e.g., polyetheretherketone (PEEK)] that is implanted between the bones or bone grafts of the spine, to provide mechanical stability and sufficient space for bone fusion to occur. Disposable devices associated with implantation may be included. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Device Size Text, specify | 0 | |
| Device Size Text, specify | 0 | |
| Device Size Text, specify | 0 |
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
- 1
- Lot or batch
- true
- Expiration date on label
- true
Other Devices From This Company#
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|---|---|---|---|---|
| 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 |
| 04038653013845 | AESCULAP | OP297R | OP297R | 2017-07-31 |
| 04038653081141 | AESCULAP | OP913 | OP913 | 2016-09-23 |
| 04038653081158 | AESCULAP | OP914 | OP914 | 2020-08-10 |
| 04038653013852 | AESCULAP | OP298R | OP298R | 2020-04-17 |
| 04046963730109 | AESCULAP | OP923 | OP923 | 2019-04-30 |
| 04046955273508 | AICON | JJ612 | JJ612 | 2022-02-25 |
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| 07613153046196 | AVS PL | Stryker Corporation | MAX | 2015-09-14 |
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| 07613153046325 | AVS PL | Stryker Corporation | MAX | 2015-09-14 |
| 07613153046332 | AVS PL | Stryker Corporation | MAX | 2015-09-14 |
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| 07613153046622 | AVS TL | Stryker Corporation | MAX | 2015-09-14 |
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