Primary Device ID | 09120047308455 |
NIH Device Record Key | f2cdd167-8f0a-45a9-b42d-fb46b1d872af |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Awl |
Version Model Number | 1-1902 |
Catalog Number | 1-1902 |
Company DUNS | 303456917 |
Company Name | I.T.S. GmbH |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | MR Safe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 09120047308455 [Primary] |
HWJ | Awl |
Steralize Prior To Use | true |
Device Is Sterile | false |
[09120047308455]
Moist Heat or Steam Sterilization
[09120047308455]
Moist Heat or Steam Sterilization
[09120047308455]
Moist Heat or Steam Sterilization
[09120047308455]
Moist Heat or Steam Sterilization
[09120047308455]
Moist Heat or Steam Sterilization
[09120047308455]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2022-06-10 |
Device Publish Date | 2018-09-17 |
09120047308455 | Awl, large |
09120047301791 | Awl, 16.0cm |