| Primary Device ID | 00817580027422 |
| NIH Device Record Key | c75823b8-5de1-44e5-8a0b-8072598bbbe3 |
| Commercial Distribution Discontinuation | 2020-07-22 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Kelyniam CSI |
| Version Model Number | PEEK-IM1004 |
| Catalog Number | PEEK-IM1004 |
| Company DUNS | 785088829 |
| Company Name | KELYNIAM GLOBAL, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Safe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | true |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | true |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00817580027422 [Primary] |
| GXN | Plate, Cranioplasty, Preformed, Non-Alterable |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00817580027422]
Moist Heat or Steam Sterilization
[00817580027422]
Moist Heat or Steam Sterilization
[00817580027422]
Moist Heat or Steam Sterilization
[00817580027422]
Moist Heat or Steam Sterilization
[00817580027422]
Moist Heat or Steam Sterilization
[00817580027422]
Moist Heat or Steam Sterilization
[00817580027422]
Moist Heat or Steam Sterilization
[00817580027422]
Moist Heat or Steam Sterilization
[00817580027422]
Moist Heat or Steam Sterilization
[00817580027422]
Moist Heat or Steam Sterilization
[00817580027422]
Moist Heat or Steam Sterilization
[00817580027422]
Moist Heat or Steam Sterilization
[00817580027422]
Moist Heat or Steam Sterilization
[00817580027422]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-07-30 |
| Device Publish Date | 2020-07-22 |
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