Primary Device ID | 05707480111619 |
NIH Device Record Key | 2842b2fe-2c15-4323-8cb9-dfaccb92c4a2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | 9" Peel-A-Way Introducer |
Version Model Number | 418000542 |
Company DUNS | 305682023 |
Company Name | Ambu A/S |
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 | true |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +14107686464 |
Purchase_orders@ambuUSA.com |
Length | 9 Inch |
Storage Environment Temperature | Between -15 Degrees Celsius and 40 Degrees Celsius |
Handling Environment Temperature | Between -50 Degrees Celsius and 50 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05707480111596 [Primary] |
GS1 | 05707480111602 [Package] Contains: 05707480111596 Package: [20 Units] In Commercial Distribution |
GS1 | 05707480111619 [Package] Contains: 05707480111602 Package: [80 Units] In Commercial Distribution |
MEB | Pump, Infusion, Elastomeric |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2017-12-20 |
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