Primary Device ID | 00852578008298 |
NIH Device Record Key | 24e78b19-ffd1-4468-9583-ec32ab7b334e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Matrix Seiff Ptosis Sling |
Version Model Number | MTX1004 |
Company DUNS | 079634199 |
Company Name | MATRIX SURGICAL HOLDINGS, LLC |
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 Issuing Agency | Device ID |
---|---|
GS1 | 00852578008298 [Primary] |
HJZ | Crutch, Ptosis |
Steralize Prior To Use | true |
Device Is Sterile | true |
[00852578008298]
Ethylene Oxide
[00852578008298]
Ethylene Oxide
[00852578008298]
Ethylene Oxide
[00852578008298]
Ethylene Oxide
[00852578008298]
Ethylene Oxide
[00852578008298]
Ethylene Oxide
[00852578008298]
Ethylene Oxide
[00852578008298]
Ethylene Oxide
[00852578008298]
Ethylene Oxide
[00852578008298]
Ethylene Oxide
[00852578008298]
Ethylene Oxide
[00852578008298]
Ethylene Oxide
[00852578008298]
Ethylene Oxide
[00852578008298]
Ethylene Oxide
[00852578008298]
Ethylene Oxide
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-06-13 |
Device Publish Date | 2025-06-05 |
00852578008298 - Matrix Seiff Ptosis Sling | 2025-06-13Seiff Ptosis Sling, used to treat blepharoptosis |
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