Primary Device ID | 50732224004247 |
NIH Device Record Key | 0684f4ef-67f0-419c-aed0-d84e225d2427 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | All-Gauze Sponges Premium |
Version Model Number | ENC2 |
Catalog Number | ENC2 |
Company DUNS | 057728685 |
Company Name | CROSSTEX INTERNATIONAL, INC. |
Device Count | 200 |
DM Exempt | true |
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 | 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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00732224004242 [Unit of Use] |
GS1 | 10732224004249 [Primary] |
GS1 | 50732224004247 [Package] Contains: 10732224004249 Package: case [25 Units] In Commercial Distribution |
EFQ | GAUZE/SPONGE, INTERNAL |
NAB | Gauze / sponge,nonresorbable for external use |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-06-30 |
Device Publish Date | 2023-06-22 |
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