Primary Device ID | 00817495024967 |
NIH Device Record Key | a7145258-1dab-49a4-83a3-dd8b7bc8da31 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Canister HFO-R1234 ZE / 950g, ALUM, 3 Pack (Japan) |
Version Model Number | FIN101106 |
Company DUNS | 053468385 |
Company Name | Candela Corporation |
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 | false |
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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00817495024967 [Primary] |
GEX | Powered Laser Surgical Instrument |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-02-12 |
Device Publish Date | 2024-02-02 |
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