Primary Device ID | 20840682102852 |
NIH Device Record Key | 7cd684fb-c6bb-4163-83b0-b144b35e94ed |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | Pedi-Lite Spirometry Kit 3m, M1032634 |
Company DUNS | 401966697 |
Company Name | GE Healthcare Finland Oy |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
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 |
Phone | +1(800)558-5120 |
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Phone | +1(800)558-5120 |
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Phone | +1(800)558-5120 |
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Phone | +1(800)558-5120 |
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Phone | +1(800)558-5120 |
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Phone | +1(800)558-5120 |
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Phone | +1(800)558-5120 |
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Phone | +1(800)558-5120 |
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Phone | +1(800)558-5120 |
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Phone | +1(800)558-5120 |
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Phone | +1(800)558-5120 |
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Phone | +1(800)558-5120 |
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Phone | +1(800)558-5120 |
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Phone | +1(800)558-5120 |
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Phone | +1(800)558-5120 |
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Phone | +1(800)558-5120 |
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Phone | +1(800)558-5120 |
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Phone | +1(800)558-5120 |
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Phone | +1(800)558-5120 |
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Phone | +1(800)558-5120 |
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Phone | +1(800)558-5120 |
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Phone | +1(800)558-5120 |
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Phone | +1(800)558-5120 |
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Phone | +1(800)558-5120 |
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Phone | +1(800)558-5120 |
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Phone | +1(800)558-5120 |
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Phone | +1(800)558-5120 |
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Device Issuing Agency | Device ID |
---|---|
GS1 | 00840682102858 [Primary] |
GS1 | 20840682102852 [Package] Contains: 00840682102858 Package: [50 Units] In Commercial Distribution |
BZK | Spirometer, monitoring (w/wo alarm) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2020-02-24 |
Device Publish Date | 2016-08-15 |
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