Primary Device ID | 04582647304414 |
NIH Device Record Key | d1181f96-d1ba-4c4d-a2dc-4ff08d3effea |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MASUNAGA M.O.C. |
Version Model Number | M.O.C. 001 C SG-C 56 |
Company DUNS | 693743585 |
Company Name | MASUNAGA OPTICAL MFG.CO.,LTD. |
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 | false |
Device Combination Product | false |
Single Use | false |
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 | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04582647304414 [Primary] |
HQY | Sunglasses (Non-Prescription Including Photosensitive) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2024-07-04 |
Device Publish Date | 2024-05-15 |
04582647304261 | M.O.C. 003 C 49 |
04582647304254 | M.O.C. 003 B 49 |
04582647304247 | M.O.C. 003 A 49 |
04582647304230 | M.O.C. 002 C 51 |
04582647304223 | M.O.C. 002 B 51 |
04582647304216 | M.O.C. 002 A 51 |
04582647304209 | M.O.C. 001 C 56 |
04582647304193 | M.O.C. 001 B 56 |
04582647304186 | M.O.C. 001 A 56 |
04582647304506 | M.O.C. 003 C SG-C 49 |
04582647304490 | M.O.C. 003 B SG-B 49 |
04582647304483 | M.O.C. 003 A SG-A 49 |
04582647304445 | M.O.C. 002 C ASG-C 51 |
04582647304438 | M.O.C. 002 B ASG-B 51 |
04582647304421 | M.O.C. 002 A ASG-A 51 |
04582647304414 | M.O.C. 001 C SG-C 56 |
04582647304407 | M.O.C. 001 B SG-B 56 |
04582647304391 | M.O.C. 001 A SG-A 56 |
04582647304476 | M.O.C. 002 C USG-C 51 |
04582647304469 | M.O.C. 002 B USG-B 51 |
04582647304452 | M.O.C. 002 A USG-A 51 |