Primary Device ID | 10884450505370 |
NIH Device Record Key | f657e6b0-dca4-46e0-8419-b0762fd3110f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | H. Lee SafeSheath® Sealing Adapter |
Version Model Number | 00884450505373 |
Catalog Number | SSSA-09 |
Company DUNS | 184763290 |
Company Name | Merit Medical Systems, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | false |
OTC Over-The-Counter | false |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00884450505373 [Primary] |
GS1 | 10884450505370 [Package] Contains: 00884450505373 Package: [5 Units] In Commercial Distribution |
DTL | Adaptor, stopcock, manifold, fitting, cardiopulmonary bypass |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-10-25 |
Device Publish Date | 2021-10-15 |
10884450505387 | 00884450505380 |
10884450505363 | 00884450505366 |
10884450505370 | 00884450505373 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
H. LEE SAFESHEATH 85417246 4138527 Live/Registered |
Pressure Products Medical Supplies Inc. 2011-09-08 |