Primary Device ID | 00850033131062 |
NIH Device Record Key | c6c6e19f-3ce6-4747-83c8-2b6aff73a31d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | RegenLab USA |
Version Model Number | RK-THT-3-20-U |
Company DUNS | 087434117 |
Company Name | Regenlab USA LLC |
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 | true |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | true |
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 | 00850033131062 [Primary] |
Steralize Prior To Use | true |
Device Is Sterile | true |
[00850033131062]
Radiation Sterilization
[00850033131062]
Radiation Sterilization
[00850033131062]
Radiation Sterilization
[00850033131062]
Radiation Sterilization
[00850033131062]
Radiation Sterilization
[00850033131062]
Radiation Sterilization
[00850033131062]
Radiation Sterilization
[00850033131062]
Radiation Sterilization
[00850033131062]
Radiation Sterilization
[00850033131062]
Radiation Sterilization
[00850033131062]
Radiation Sterilization
[00850033131062]
Radiation Sterilization
[00850033131062]
Radiation Sterilization
[00850033131062]
Radiation Sterilization
[00850033131062]
Radiation Sterilization
[00850033131062]
Radiation Sterilization
[00850033131062]
Radiation Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-05-08 |
Device Publish Date | 2023-04-28 |
00850033131086 | R-ET |
00850033131079 | RK-WG-2 |
00850033131062 | RK-THT-3-20-U |
00850033131055 | RK-THT-3-U |
00850033131048 | RK-BCT-3-20-U |
00850033131031 | RK-BCT-3-U |
00850033131109 | RegenKit-THT-BMC, Ref: RK-THT-BMC-3-10 |