Primary Device ID | 04899959015052 |
NIH Device Record Key | 70f71e56-33a8-4970-b016-b9aba11aeeb4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Belun Ring |
Version Model Number | BLR-100C |
Company DUNS | 664437924 |
Company Name | Belun Technology Company Limited |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
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 | 04899959015052 [Primary] |
DQA | Oximeter |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-01-08 |
Device Publish Date | 2020-12-31 |
04899959015069 | Belun Ring Size 13 |
04899959015052 | Belun Ring Size 11 |
04899959015045 | Belun Ring Size 10 |
04899959015038 | Belun Ring Size 9 |
04899959015021 | Belun Ring Size 7 |
04899959015014 | Belun Ring Size 5 |
04899959015090 | Belun Ring BLR-100X Size L |
04899959015083 | Belun Ring BLR-100X Size M |
04899959015076 | Belun Ring BLR-100X size S |
04899959015007 | Belun Ring BLR-100X Size F |