Primary Device ID | 16970462546426 |
NIH Device Record Key | 1ba1684e-e7fd-4159-a81d-7225c140c99f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Single-Use Rhinolaryngoscope |
Version Model Number | RH-M58H |
Company DUNS | 403655303 |
Company Name | Shenzhen HugeMed Medical Technical Development Co., Ltd. |
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 | false |
Serial Number | true |
Manufacturing Date | true |
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 | 06970462546429 [Primary] |
GS1 | 16970462546426 [Package] Contains: 06970462546429 Package: CASE [10 Units] Discontinued: 2024-06-11 Not in Commercial Distribution |
GS1 | 26970462546423 [Package] Contains: 06970462546429 Package: CASE [5 Units] Discontinued: 2024-06-11 Not in Commercial Distribution |
EOB | Nasopharyngoscope (Flexible Or Rigid) |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-06-19 |
Device Publish Date | 2024-06-11 |
16970462546488 | RH-M32A |
16970462546440 | RH-M40H |
16970462546433 | RH-M52H |
16970462546426 | RH-M58H |
16970462546419 | RH-M22 |
16970462546402 | RH-M32 |
16970462546396 | RH-M40 |
16970462546389 | RH-M50 |
16970462546372 | RH-M52 |
16970462546365 | RH-M58 |