Primary Device ID | 00383730001173 |
NIH Device Record Key | c0a75369-3210-4c17-8c9c-72e28509663e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MASK - OC ADV |
Version Model Number | 00 |
Catalog Number | HS81211-010 |
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 | 00383730001173 [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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00383730004501 - I-neb Clinical Study Disc | 2020-04-01 I-neb Clinical Study Disc |
00383730004518 - I-neb Generic ClinicalStudy Disc Power10 | 2020-04-01 I-neb Generic Clinical Study Disc Power10 |
00383730004587 - I-neb In Vitro Test Disc Power 10 | 2020-04-01 I-neb In Vitro Test Disc Power 10 |