Primary Device ID | 00844685002221 |
NIH Device Record Key | bdb0889d-9def-41ee-b31f-4e1a101e1949 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Luer Adaptor Tip, Irr., For InterTip™ Stainless I/A System |
Version Model Number | IH-90308 |
Catalog Number | IH-90308 |
Company DUNS | 097824130 |
Company Name | MICROSURGICAL TECHNOLOGY, INC. |
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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00844685002221 [Primary] |
HMX | Cannula, Ophthalmic |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00844685002221]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-10-07 |
Device Publish Date | 2018-09-16 |
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