Primary Device ID | 10884450282530 |
NIH Device Record Key | 3c0a5ed4-8832-4e30-974d-9fb857a8fe8b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PAL™ |
Version Model Number | 00884450282533 |
Catalog Number | PAL225/A |
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 | false |
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 Issuing Agency | Device ID |
---|---|
GS1 | 00884450282533 [Primary] |
GS1 | 10884450282530 [Package] Contains: 00884450282533 Package: [25 Units] In Commercial Distribution |
GS1 | 20884450282537 [Package] Package: [4 Units] In Commercial Distribution |
LYV | LABEL OR TAG, STERILE |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2018-02-16 |
10884450282639 | 00884450282632 |
10884450282622 | 00884450282625 |
10884450282608 | 00884450282601 |
10884450282592 | 00884450282595 |
20884450282582 | 00884450282588 |
10884450282578 | 00884450282571 |
10884450282561 | 00884450282564 |
20884450282551 | 00884450282557 |
20884450282544 | 00884450282540 |
10884450282530 | 00884450282533 |
20884450282520 | 00884450282526 |
20884450282513 | 00884450282519 |
20884450055148 | 00884450055144 |
20884450282612 | 00884450282618 |
10884450834050 | B |
10884450834111 | B |
10884450834098 | B |
20884450834088 | B |
10884450834043 | B |