Primary Device ID | 04546540755902 |
NIH Device Record Key | 1f2afc4d-68d8-4983-87ce-5e0409dec11c |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 234-020-093 |
Catalog Number | 234-020-093 |
Company DUNS | 187502109 |
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 | false |
Lot Batch | true |
Serial Number | false |
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(866)624-4422 |
xx@xx.xx |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04546540755902 [Primary] |
HRT | STRIPPER, SURGICAL |
Steralize Prior To Use | true |
Device Is Sterile | false |
[04546540755902]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2015-09-04 |
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