Primary Device ID | 18437006085059 |
NIH Device Record Key | b6b05e98-35aa-46b5-8a23-b90d938f91f9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Cranial LOOP L |
Version Model Number | FC050100 |
Company DUNS | 465890437 |
Company Name | NEOS SURGERY SL |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 093 594 4726 |
info@neosurgery.com | |
Phone | 093 594 4726 |
info@neosurgery.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 18437006085059 [Primary] |
GS1 | 28437006085056 [Package] Package: [64 Units] In Commercial Distribution |
GS1 | 38437006085053 [Package] Package: [6 Units] In Commercial Distribution |
GS1 | 48437006085050 [Package] Contains: 38437006085053 Package: [10 Units] In Commercial Distribution |
GXR | Cover, Burr Hole |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-02-04 |
08437006085182 - Depth Gauge | 2024-09-12 DEPTH GAUGE |
08437006085212 - Retractor | 2024-09-12 |
08437006085434 - Cutter | 2024-09-12 |
28437006085452 - STERN FIX | 2024-09-12 STERN FIX Sternal Stabilization System, Size 2 |
28437006085469 - STERN FIX | 2024-09-12 STERN FIX Sternal Stabilization System- size 3 |
08437006085472 - STERN FIX | 2024-09-12 STERN FIX Sternal Stabilization System-Size 4 |
28437006085483 - STERN FIX | 2024-09-12 STERN FIX Sternal Stabilization System- Size 5 |
08437006085496 - Forceps | 2024-09-12 |