Primary Device ID | 00888937018240 |
NIH Device Record Key | ee90e09d-0a19-4b6b-95bf-c5c9313d4b25 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Lone Star® IRI Delivery |
Version Model Number | IRI-DTD |
Company DUNS | 801895244 |
Company Name | Coopersurgical, Inc. |
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 | 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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00888937018240 [Primary] |
KOA | Surgical Instruments, G-U, Manual (And Accessories) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-07-01 |
Device Publish Date | 2024-06-21 |
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