Primary Device ID | 00518021000007 |
NIH Device Record Key | a95f291c-24ee-4fd6-a748-211f0e9ee3e2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | C Relief |
Version Model Number | TENS |
Company DUNS | 421286946 |
Company Name | Hong Qiangxing (Shen Zhen) Electronics Limited |
Device Count | 8 |
DM Exempt | true |
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 | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00518021000007 [Primary] |
GS1 | 00518021000008 [Unit of Use] |
GZJ | Stimulator, Nerve, Transcutaneous, For Pain Relief |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2019-10-23 |
Device Publish Date | 2018-01-08 |
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06971712727889 - NEOCARBON | 2024-11-07 |
06971712720033 - Epulse | 2024-11-04 Mini Massager ULTRA 1420 |
06971712727681 - Chirp | 2024-11-01 |
06971712727698 - Chirp | 2024-11-01 |
06971712727728 - Chirp | 2024-11-01 |
06971712727735 - Beemoon | 2024-11-01 |
06971712727858 - NEOCARBON | 2024-10-31 |