Primary Device ID | 05023323029515 |
NIH Device Record Key | 517d885e-7973-4b00-a70e-961c9cdd87dd |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Clement Clarke International |
Version Model Number | 3103095 |
Company DUNS | 216155952 |
Company Name | CLEMENT CLARKE INTERNATIONAL LIMITED |
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 | true |
Serial Number | false |
Manufacturing Date | true |
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 | 05023323001160 [Package] Package: [40 Units] In Commercial Distribution |
GS1 | 05023323029515 [Package] Contains: 05023323029522 Package: [15 Units] In Commercial Distribution |
GS1 | 05023323029522 [Primary] |
BYP | Mouthpiece, Breathing |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-12-13 |
Device Publish Date | 2022-12-05 |
05023323029515 | UNIVERSAL M/PIECES IN BAG X15 |
05023323029492 | O:W:VAL:PAED:M/PCE:ADAPT:PK 20 |
05023323001344 | ONE WAY VALVE EXP (500) |
05023323000491 | ONE WAY VALVE EXP (200) |
05023323000507 | ONE WAY VALVE INSPIRATORY (200) |
05023323001559 | ONE WAY VALVE: EXP (5X20) |
05023323001191 | ONE WAY VALVE INSP (500) |
05023323001085 | ONE WAY VALVE INSPIRATORY (5X20) |