Primary Device ID | 04546540216458 |
NIH Device Record Key | e0b01365-0f2a-4c05-ae36-0f8fb33e3ef2 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 4103160000 |
Catalog Number | 4103-160-000 |
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 | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | false |
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 | 04546540216458 [Primary] |
KIJ | INSTRUMENT, SURGICAL, ORTHOPEDIC, DC-POWERED MOTOR AND ACCESSORY/ATTACHMENT |
Steralize Prior To Use | true |
Device Is Sterile | false |
[04546540216458]
Ethylene Oxide
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2020-01-20 |
Device Publish Date | 2018-09-24 |
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07613327616675 - SPY | 2024-03-06 |