Primary Device ID | 37613252051108 |
NIH Device Record Key | b36b4d0f-2f65-429b-a68c-88cd9a1b9b49 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 5450800316 |
Catalog Number | 5450800316 |
Company DUNS | 196548481 |
Company Name | STRYKER CORPORATION |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
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 Issuing Agency | Device ID |
---|---|
GS1 | 07613252051107 [Primary] |
GS1 | 37613252051108 [Package] Contains: 07613252051107 Package: pack [5 Units] In Commercial Distribution |
LFL | Instrument, ultrasonic surgical |
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 | 2016-09-23 |
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