Primary Device ID | 07613327262889 |
NIH Device Record Key | b3b020e5-d184-40c2-ae03-36d7d1e3da0e |
Commercial Distribution Discontinuation | 2025-03-17 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | XIA II |
Version Model Number | 48040100 |
Catalog Number | 48040100 |
Company DUNS | 149183167 |
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 | true |
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 | 07613327262889 [Primary] |
HAO | INSTRUMENT, SURGICAL, NON-POWERED |
Steralize Prior To Use | true |
Device Is Sterile | false |
[07613327262889]
Moist Heat or Steam Sterilization
[07613327262889]
Moist Heat or Steam Sterilization
[07613327262889]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2025-03-10 |
Device Publish Date | 2019-11-21 |
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