Primary Device ID | 50649111493278 |
NIH Device Record Key | cbe50e6b-d414-4ced-8031-2bd50c980c21 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Trinity Sterile, Inc. |
Version Model Number | 96-4921A |
Company DUNS | 006966006 |
Company Name | SKLAR CORPORATION |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10649111493270 [Primary] |
GS1 | 50649111493278 [Package] Contains: 10649111493270 Package: [25 Units] In Commercial Distribution |
HTD | FORCEPS |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-12-20 |
Device Publish Date | 2024-12-12 |
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