Primary Device ID | 16973062320069 |
NIH Device Record Key | cb4ca2a7-75b3-4aa3-bc03-d9b6e7d642ee |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Standard Surgical Gown (AAMI Level 3) |
Version Model Number | PM5002SGS |
Company DUNS | 529796225 |
Company Name | Foshan Nanhai Plus Medical 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 | true |
Serial Number | false |
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 | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06973062320062 [Primary] |
GS1 | 16973062320069 [Package] Contains: 06973062320062 Package: [50 Units] In Commercial Distribution |
FYA | Gown, Surgical |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-09-08 |
Device Publish Date | 2021-08-31 |
16973062320090 | PM5005SGS |
16973062320083 | PM5004SGS |
16973062320076 | PM5003SGS |
16973062320069 | PM5002SGS |
16973062320052 | PM5001SGS |
06973062320048 | PM5005SGN |
06973062320031 | PM5004SGN |
06973062320024 | PM5003SGN |
06973062320017 | PM5002SGN |
06973062320000 | PM5001SGN |
16973062320298 | PM5015SGS |
16973062320281 | PM5014SGS |
16973062320274 | PM5013SGS |
16973062320267 | PM5012SGS |
06973062320253 | PM5011SGS |
06973062320246 | PM5015SGN |
06973062320239 | PM5014SGN |
06973062320222 | PM5013SGN |
06973062320215 | PM5012SGN |
06973062320208 | PM5011SGN |