MEDPOR TITAN
- Primary DI
- 07613252084365
- Brand
- MEDPOR TITAN
- Company
- Stryker Leibinger GmbH & Co. KG
- Model
- 81035
- Catalog number
- 81035
- Device description
- MAX Orbital Floor and Wall MTB Left
- Published
- 2015-09-24
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- Sterile
- true
- Single use
- true
Product Codes#
| Code | Name |
|---|---|
| FTM | Mesh, surgical |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| FTM | Mesh, Surgical | General, Plastic Surgery | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K040364 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 07613252084365 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 07613252084365 | 07613252084365 | 7613252084365 |
GMDN Terms#
| Term | Definition |
|---|---|
| Polyethylene craniofacial tissue reconstructive material | A sterile implantable device intended to support, contour, and provide structure for the craniofacial anatomy (i.e., head and face including the chin, cheeks, nose, eye sockets and ears) during reconstructive and plastic surgery procedures. It is typically a high-density polyethylene (PE) material with an interconnecting pore structure that supports tissue ingrowth. The device is available in blocks, sheets, wedges and spheres that can be cut by the surgeon to meet the patient's specific needs. This is a single-use device. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Device Size Text, specify | 0 | |
| Length | 41 | Millimeter |
| Width | 1 | Millimeter |
| Width | 42 | Millimeter |
Sterilization Methods#
| Method |
|---|
Regulatory Flags#
- DUNS number
- 316153956
- Device count
- 1
- Lot or batch
- true
- Manufacturing date on label
- true
- Expiration date on label
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 37613327122962 | NA | 29-93003 | 29-93003 | 2018-04-13 |
| 04546540274250 | NA | 64-00132 | 64-00132 | 2017-01-11 |
| 07613327122893 | NA | 29-93001 | 29-93001 | 2017-12-01 |
| 07613327122909 | NA | 29-92001 | 29-92001 | 2017-03-31 |
| 07613327122916 | NA | 29-92003 | 29-92003 | 2017-03-31 |
| 07613327122930 | NA | 29-92002 | 29-92002 | 2017-03-31 |
| 07613327122947 | NA | 29-91002 | 29-91002 | 2017-03-31 |
| 07613327122978 | NA | 29-93002 | 29-93002 | 2017-12-01 |
| 07613327123326 | NA | 29-92004 | 29-92004 | 2017-03-31 |
| 37613154881872 | PINABALL | 6003-003-090 | 6003-003-090 | 2016-09-21 |
| 57613252088436 | TLS, Quintube | 6630 | 6630 | 2016-08-24 |
| 07613327465532 | NA | 92-00232 | 92-00232 | 2019-05-03 |
| 07613327465549 | NA | 92-00230 | 92-00230 | 2019-05-03 |
| 04546540134790 | NA | 01-03230 | 01-03230 | 2017-01-11 |
| 04546540134974 | NA | 01-04010 | 01-04010 | 2016-12-08 |
| 04546540134998 | NA | 01-04070 | 01-04070 | 2016-12-08 |
| 04546540135018 | NA | 01-04100 | 01-04100 | 2016-12-08 |
| 04546540138477 | NA | 01-09561 | 01-09561 | 2016-12-08 |
| 04546540141514 | NA | 01-15315 | 01-15315 | 2017-01-11 |
| 04546540143242 | NA | 01-19715 | 01-19715 | 2016-12-08 |
Other Devices Sharing Product Codes#
| Primary DI | Brand | Company | Product code | Published |
|---|---|---|---|---|
| 00802526629907 | CanGaroo® | Boston Scientific Corporation | FTM | 2026-05-27 |
| 00802526629914 | CanGaroo® | Boston Scientific Corporation | FTM | 2026-05-27 |
| 00802526629921 | CanGaroo® | Boston Scientific Corporation | FTM | 2026-05-27 |
| 00802526629938 | CanGaroo® | Boston Scientific Corporation | FTM | 2026-05-27 |
| 00802526629945 | CanGaroo® | Boston Scientific Corporation | FTM | 2026-05-27 |
| 00802526630002 | EluPro™ | Boston Scientific Corporation | FTM | 2026-05-27 |
| 00802526630019 | EluPro™ | Boston Scientific Corporation | FTM | 2026-05-27 |
| 09421908222393 | Myriad Matrix™ Restore Restorative Bioscaffold | AROA BIOSURGERY LIMITED | FTM | 2026-01-30 |
| 09421908222416 | Myriad Matrix™ Restore Restorative Bioscaffold | AROA BIOSURGERY LIMITED | FTM | 2026-01-30 |
| 09421908222430 | Myriad Matrix™ Restore Restorative Bioscaffold | AROA BIOSURGERY LIMITED | FTM | 2026-01-30 |
| 09421908222454 | Myriad Matrix™ Restore Restorative Bioscaffold | AROA BIOSURGERY LIMITED | FTM | 2026-01-30 |
| 09421907331881 | OviTex® Core | AROA BIOSURGERY LIMITED | FTM | 2025-11-26 |
| 09421907331935 | OviTex® 1S | AROA BIOSURGERY LIMITED | FTM | 2025-11-26 |
| 09421907331942 | OviTex® 1S | AROA BIOSURGERY LIMITED | FTM | 2025-11-26 |
| 09421907331959 | OviTex® 1S | AROA BIOSURGERY LIMITED | FTM | 2025-11-26 |
| 09421907331973 | OviTex® 1S | AROA BIOSURGERY LIMITED | FTM | 2025-11-26 |
| 09421908222065 | OviTex® 2S | AROA BIOSURGERY LIMITED | FTM | 2025-11-26 |
| 09421908222096 | OviTex® Low Profile | AROA BIOSURGERY LIMITED | FTM | 2025-11-26 |
| 09421908222102 | OviTex® Low Profile | AROA BIOSURGERY LIMITED | FTM | 2025-11-26 |
| 09421908222157 | OviTex® Inguinal | AROA BIOSURGERY LIMITED | FTM | 2025-11-26 |
| 00085412658681 | Peri-Strips Dry with Veritas | SYNOVIS LIFE TECHNOLOGIES, INC. | FTM | 2024-11-21 |
| 00085412658834 | Peri-Strips Dry with Veritas | SYNOVIS LIFE TECHNOLOGIES, INC. | FTM | 2024-11-21 |
| B454VSC10 | VersaWrap | Alafair Biosciences, Inc. | FTM | 2024-06-10 |
| 09421906661903 | OviTex® IHR | AROA BIOSURGERY LIMITED | FTM | 2024-03-21 |
| 09421906661910 | OviTex® IHR | AROA BIOSURGERY LIMITED | FTM | 2024-03-21 |
| 09421906661927 | OviTex® IHR | AROA BIOSURGERY LIMITED | FTM | 2024-03-21 |
| 00085412818375 | Supple Peri-Guard | SYNOVIS LIFE TECHNOLOGIES, INC. | FTM | 2023-05-15 |
| 00085412818405 | Peri-Guard | SYNOVIS LIFE TECHNOLOGIES, INC. | FTM | 2023-05-15 |
| 00085412818429 | Supple Peri-Guard | SYNOVIS LIFE TECHNOLOGIES, INC. | FTM | 2023-05-15 |
| 00085412818443 | Peri-Guard | SYNOVIS LIFE TECHNOLOGIES, INC. | FTM | 2023-05-15 |