Primary Device ID | 00850027193175 |
NIH Device Record Key | e7f266b6-993c-49c5-be1e-6fde2931acac |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Polyester Spun Swab 50ct. Pouch |
Version Model Number | 60632 |
Company DUNS | 042126640 |
Company Name | Steripack (usa) Limited LLC |
Device Count | 50 |
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 | true |
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 | 00850027193175 [Package] Contains: 00850027193335 Package: Case Box [2000 Units] In Commercial Distribution |
GS1 | 00850027193199 [Unit of Use] |
GS1 | 00850027193335 [Primary] |
KXG | Applicator, Absorbent Tipped, Sterile |
Steralize Prior To Use | true |
Device Is Sterile | true |
[00850027193175]
Radiation Sterilization
[00850027193175]
Radiation Sterilization
[00850027193175]
Radiation Sterilization
[00850027193175]
Radiation Sterilization
[00850027193175]
Radiation Sterilization
[00850027193175]
Radiation Sterilization
[00850027193175]
Radiation Sterilization
[00850027193175]
Radiation Sterilization
[00850027193175]
Radiation Sterilization
[00850027193175]
Radiation Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-10-11 |
Device Publish Date | 2022-10-03 |
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