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1.1 This guide addresses the determination of appropriate device attributes for testing as part of a shelf-life study for endovascular devices. Combination and biodegradable devices (for example drug-devices, biologic devices or drug biologics) may require additional considerations, depending on their nature.
| Author | ASTM |
|---|---|
| Editor | ASTM |
| Document type | Standard |
| Format | File |
| Confirmation date | 2018-11-01 |
| ICS | 11.040.40 : Implants for surgery, prosthetics and orthotics
|
| Number of pages | 6 |
| Replace | ASTM F2914-12 |
| Set | ASTMVOL1302 |
| Year | 2012 |
| Document history | ASTM F2914-12 |
| Country | USA |
| Keyword | ASTM 2914;ASTM F2914;ASTM F2914;10.1520/F2914-12R18 |