Primary Device ID | 00731124001252 |
NIH Device Record Key | 356e9e4a-e927-42bd-89e4-ac01e30e38af |
Commercial Distribution Discontinuation | 2019-07-15 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Safer Pain Relief Sales Kit |
Version Model Number | 14210 |
Company DUNS | 004163390 |
Company Name | HYGENIC CORPORATION, THE |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | true |
Device Combination Product | true |
Single Use | true |
Lot Batch | false |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00731124001252 [Primary] |
KGX | Tape And Bandage, Adhesive |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2019-10-23 |
Device Publish Date | 2019-07-15 |
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