Primary Device ID | 37613327117050 |
NIH Device Record Key | e33c08a0-4727-4272-9569-fa6956a5b4d5 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 5100901908 |
Catalog Number | 5100-901-908 |
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 | 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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07613327117059 [Primary] |
GS1 | 37613327117050 [Package] Contains: 07613327117059 Package: pack [2 Units] In Commercial Distribution |
EIA | UNIT, OPERATIVE DENTAL |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 8 |
Public Version Date | 2020-01-20 |
Device Publish Date | 2016-09-23 |
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