Primary Device ID | 10852367007003 |
NIH Device Record Key | 9940f535-2db6-45f7-9b4c-6771685cf981 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | InspiraChamber Valved Holding Chamber |
Version Model Number | IC-VHC-0 |
Company DUNS | 967174850 |
Company Name | INSPIRX, INC |
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 | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00852367007006 [Primary] |
GS1 | 10852367007003 [Package] Contains: 00852367007006 Package: [50 Units] In Commercial Distribution |
NVP | Holding Chambers, Direct Patient Interface |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2017-12-18 |
10852367007003 | InspiraChamber Anti-Static Valved Holding Chamber- Hospital Unit |
10852367007065 | InspiraChamber Anti-Static Valved Holding Chamber (Teleflex medical) 1001-50 |
10852367007058 | InspiraChamber Anti-Static Valved Holding Chamber (Teleflex Medical) 1001-10 |
10852367007164 | InspiraChamber with InspiraMask (Small) (Teleflex Medical) 1001-10S |
10852367007157 | InspiraChamber with InspiraMask (Medium) (Teleflex Medical) 1001-10M |
10852367007133 | InspiraChamber with SootherMask (Medium) (Teleflex Medical) 1001-10SM |
10852367007126 | InspiraChamber with InspiraMask (Large) (Teleflex Medical) 1001-10L |
10852367007072 | InspiraChamber with SootherMask (Small) (Teleflex Medical) 1001-10SS |