Primary Device ID | 24053613291846 |
NIH Device Record Key | 693d68b5-916e-421e-9241-9815c59580f5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Guide Pin |
Version Model Number | HTS-4P-03-090 |
Catalog Number | HTS-4P-03-090 |
Company DUNS | 317409001 |
Company Name | Gebr. Brasseler GmbH & Co. KG |
Device Count | 4 |
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 | true |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 14053613291849 [Primary] |
GS1 | 24053613291846 [Package] Contains: 14053613291849 Package: [1 Units] In Commercial Distribution |
GS1 | 84053613291848 [Unit of Use] |
HWC | Screw, Fixation, Bone |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-10-10 |
Device Publish Date | 2024-10-02 |
24053613285968 | Guide Pin Ø 3,20mm |
24053613285944 | Guide Pin Ø 3,20mm |
24053613285937 | Guide Pin Ø 3,20mm |
24053613291990 | HTZ-2P-020-00 |
24053613291891 | HTZ-4P-020-00 |
24053613291846 | HTS-4P-03-090 |
24053613292041 | HTSN-2P-76032 |
24053613291907 | HTD-4P-02-300 |
24053613291839 | HTS-4P-2038A |