Primary Device ID | 16973062320199 |
NIH Device Record Key | 11e1245f-2334-452b-8849-d5a91ffb27a0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Reinforce Surgical Gown (AAMI Level 3) |
Version Model Number | PM5005RGS |
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 | 06973062320192 [Primary] |
GS1 | 16973062320199 [Package] Contains: 06973062320192 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 |
16973062320199 | PM5005RGS |
16973062320182 | PM5004RGS |
16973062320175 | PM5003RGS |
16973062320168 | PM5002RGS |
16973062320151 | PM5001RGS |
06973062320147 | PM5005RGN |
06973062320130 | PM5004RGN |
06973062320123 | PM5003RGN |
06973062320116 | PM5002RGN |
06973062320109 | PM5001RGN |
16973062320397 | PM5015RGS |
16973062320380 | PM5014RGS |
16973062320373 | PM5013RGS |
16973062320366 | PM5012RGS |
16973062320359 | PM5011RGS |
06973062320345 | PM5015RGN |
06973062320338 | PM5014RGN |
06973062320321 | PM5013RGN |
06973062320314 | PM5012RGN |
06973062320307 | PM5011RGN |