Primary Device ID | 00850027193199 |
NIH Device Record Key | b0392b06-9c1e-421c-b1bd-5eb30019836d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Sterile Polyester Spun Swab |
Version Model Number | 60564 |
Company DUNS | 042126640 |
Company Name | Steripack (usa) Limited LLC |
Device Count | 2000 |
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 | 00850027193199 [Unit of Use] |
GS1 | 00860004112716 [Primary] |
KXG | Applicator, Absorbent Tipped, Sterile |
Steralize Prior To Use | true |
Device Is Sterile | true |
[00850027193199]
Radiation Sterilization
[00850027193199]
Radiation Sterilization
[00850027193199]
Radiation Sterilization
[00850027193199]
Radiation Sterilization
[00850027193199]
Radiation Sterilization
[00850027193199]
Radiation Sterilization
[00850027193199]
Radiation Sterilization
[00850027193199]
Radiation Sterilization
[00850027193199]
Radiation Sterilization
[00850027193199]
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 |
00860004112716 | single use, sterile pouched polyester spun swabs for specimen ciollection sampling from nasal ar |
00850027193199 | single use, sterile pouched polyester spun swabs for specimen ciollection sampling from nasal ar |