Primary Device ID | 80618125190368 |
NIH Device Record Key | 1fb15372-f32b-466d-87fd-8e5df5a726cd |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AquaGuard |
Version Model Number | 50011-RPK |
Catalog Number | 50011-RPK |
Company DUNS | 063519193 |
Company Name | TIDI PRODUCTS, LLC |
Device Count | 5 |
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 | true |
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 | false |
OTC Over-The-Counter | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00618125190362 [Primary] |
GS1 | 80618125190368 [Unit of Use] |
KGX | Tape And Bandage, Adhesive |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-08-11 |
Device Publish Date | 2023-08-03 |
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80618125190337 | TIDI Moisture Barrier Clear Polyethylene 98 per Case |
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80618125190313 | TIDI Moisture Barrier Clear Polyethylene 98 per Case |
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80618125190283 | TIDI Moisture Barrier Clear Polyethylene 98 per Case |
80618125190269 | TIDI Moisture Barrier Clear Polyethylene 5 per Package |
80618125190252 | TIDI Moisture Barrier Clear Polyethylene 98 per Case |