Primary Device ID | 00863221000309 |
NIH Device Record Key | 4c0646f2-6da1-4c36-b0e5-25598f7dcc1a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SkinPen |
Version Model Number | 014 |
Company DUNS | 005677967 |
Company Name | BELLUS MEDICAL, 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 | 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 | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00863221000309 [Primary] |
QAI | Powered Microneedle Device |
Steralize Prior To Use | true |
Device Is Sterile | true |
[00863221000309]
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Public Version Status | New |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2018-04-09 |
00863221000361 | 1 |
00863221000354 | 24 count of Treatment Kit singles |
00863221000347 | 101 |
00863221000330 | SkinPen Box (includes SkinPen Precision hand-piece, charging base, and AC Adapter). |
00863221000323 | Treatment kit which includes a sterile, disposable cartridge tip, a hydrogel 510k exempt medical |
00863221000316 | 100 |
00863221000309 | 014 |
20863221000327 | Case of 18 single treatment kits. |
10863221000320 | Case of 12 SkinPen Precision Treatment Kits |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SKINPEN 85922262 4532187 Live/Registered |
Bellus Medical, LLC 2013-05-03 |