Primary Device ID | 05030267011315 |
NIH Device Record Key | d713c73c-ea39-4b0a-8b44-8e6b6553418e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | LUER ELBOW, 7.6MM PORT |
Version Model Number | 2710000 |
Company DUNS | 785952607 |
Company Name | Intersurgical Incorporated |
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 | true |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05030267011315 [Package] Contains: 05030267064502 Package: [25 Units] In Commercial Distribution |
GS1 | 05030267064502 [Primary] |
GS1 | 05030267090037 [Package] Contains: 05030267064502 Package: [100 Units] In Commercial Distribution |
BZA | Connector, Airway (Extension) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-06-23 |
Device Publish Date | 2023-06-15 |
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