Primary Device ID | 00810125923494 |
NIH Device Record Key | 2252ef11-3341-4773-9809-383a1cf70309 |
Commercial Distribution Discontinuation | 2023-12-08 |
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 | 00810125923494 [Primary] |
GXN | Plate, Cranioplasty, Preformed, Non-Alterable |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00810125923494]
Moist Heat or Steam Sterilization
[00810125923494]
Moist Heat or Steam Sterilization
[00810125923494]
Moist Heat or Steam Sterilization
[00810125923494]
Moist Heat or Steam Sterilization
[00810125923494]
Moist Heat or Steam Sterilization
[00810125923494]
Moist Heat or Steam Sterilization
[00810125923494]
Moist Heat or Steam Sterilization
[00810125923494]
Moist Heat or Steam Sterilization
[00810125923494]
Moist Heat or Steam Sterilization
[00810125923494]
Moist Heat or Steam Sterilization
[00810125923494]
Moist Heat or Steam Sterilization
[00810125923494]
Moist Heat or Steam Sterilization
[00810125923494]
Moist Heat or Steam Sterilization
[00810125923494]
Moist Heat or Steam Sterilization
[00810125923494]
Moist Heat or Steam Sterilization
[00810125923494]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-12-18 |
Device Publish Date | 2023-12-08 |
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