| Primary Device ID | 00383730000459 |
| NIH Device Record Key | 55f6311f-e9f0-4962-8b09-2a6d195787dc |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PERSONAL BEST |
| Version Model Number | 00 |
| Catalog Number | HS756 |
| 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 | false |
| OTC Over-The-Counter | true |
| Phone | +1(724)744-2500 |
| respironics.service@philips.com | |
| Phone | +1(724)744-2500 |
| respironics.service@philips.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00383730000459 [Primary] |
| BZH | METER, PEAK FLOW, SPIROMETRY |
| 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 |
| 00383730000480 | PERSONAL BEST LR PFM (756EU)-CEG |
| 00383730000473 | PERSONAL BEST LR PFM (756)-12PK |
| 00383730000466 | PERSONAL BEST LR PFM-RUSSIA-SINGLE UNIT |
| 00383730000459 | PERSONAL BEST LR PFM ASSY |
| 00383730000442 | PERSONAL BEST FR PFM-RUSSIA-SINGLE UNIT |
| 00383730000435 | PERSONAL BEST FR PFM (755) - 12PK |
| 00383730000428 | PERSONAL BEST FR PFM ASSY |
| 00383730000411 | PERSONAL BEST FR PFM - CEGLA (ISO 23747) |
| 00383730000404 | PERSONAL BEST FR PFM ISO-23747 SINGLE |
| 00383730000398 | PERSONAL BEST ISO ASSEMBLY |