Primary Device ID | 34546540185021 |
NIH Device Record Key | 445e197d-69e6-465e-8332-9d094b3d9841 |
Commercial Distribution Discontinuation | 2019-04-01 |
Commercial Distribution Status | Not in Commercial Distribution |
Version Model Number | 0215031000 |
Catalog Number | 0215-031-000 |
Company DUNS | 196548481 |
Company Name | STRYKER CORPORATION |
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 | true |
OTC Over-The-Counter | false |
Phone | +1(800)253-3210 |
Inst.Stryker.cs@Stryker.com |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04546540185020 [Primary] |
GS1 | 34546540185021 [Package] Contains: 04546540185020 Package: pack [10 Units] Discontinued: 2019-04-01 Not in Commercial Distribution |
GCY | APPARATUS, SUCTION, SINGLE PATIENT USE, PORTABLE, NONPOWERED |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2020-02-19 |
Device Publish Date | 2018-09-24 |
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