Primary Device ID | 00383730001159 |
NIH Device Record Key | 35bac0a4-0f48-48d8-b4ce-10adf59c2458 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MASK - OC Advanced |
Version Model Number | 00 |
Catalog Number | HS81211 |
Company DUNS | 220018415 |
Company Name | RESPIRONICS RESPIRATORY DRUG DELIVERY (UK) 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 | false |
Lot Batch | true |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00383730001159 [Primary] |
CAF | NEBULIZER (DIRECT PATIENT INTERFACE) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-08-24 |
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00383730001197 | Oc Advanced Lark Mask (81310EU), Single Unit |
00383730001180 | OC Advanced Adult Large Mask |
00383730001166 | OC Advanced Medium Pediatric Mask, Single Unit |
00383730001159 | OC Advanced Pediatric Medium Mask |
00383730001142 | OC Advanced Pediatric Small Mask |
00383730001135 | OC Advanced Small Pediatric Mask, Single Unit |
00383730001128 | OC Advanced Pediatric Small Mask |