UNIVERSAL FLEX2® DF370-6131Z
GUDID 00612649213842
UNIVERSAL FLEX2 CIRCUIT
King Systems Corporation
Anaesthesia breathing circuit, single-use| Primary Device ID | 00612649213842 |
| NIH Device Record Key | 3d8bd144-2eab-4208-a500-87cb8b617f77 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | UNIVERSAL FLEX2® |
| Version Model Number | DF370-6131Z |
| Catalog Number | DF370-6131Z |
| Company DUNS | 009299017 |
| Company Name | King Systems Corporation |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | 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 |
Customer Support Contacts
| Phone | +14107686464 |
| Purchase_orders@ambuUSA.com | |
| Phone | +14107686464 |
| Purchase_orders@ambuUSA.com | |
| Phone | +14107686464 |
| Purchase_orders@ambuUSA.com | |
| Phone | +14107686464 |
| Purchase_orders@ambuUSA.com | |
| Phone | +14107686464 |
| Purchase_orders@ambuUSA.com | |
| Phone | +14107686464 |
| Purchase_orders@ambuUSA.com | |
| Phone | +14107686464 |
| Purchase_orders@ambuUSA.com | |
| Phone | +14107686464 |
| Purchase_orders@ambuUSA.com | |
| Phone | +14107686464 |
| Purchase_orders@ambuUSA.com | |
| Phone | +14107686464 |
| Purchase_orders@ambuUSA.com | |
| Phone | +14107686464 |
| Purchase_orders@ambuUSA.com | |
| Phone | +14107686464 |
| Purchase_orders@ambuUSA.com | |
| Phone | +14107686464 |
| Purchase_orders@ambuUSA.com | |
| Phone | +14107686464 |
| Purchase_orders@ambuUSA.com | |
| Phone | +14107686464 |
| Purchase_orders@ambuUSA.com | |
| Phone | +14107686464 |
| Purchase_orders@ambuUSA.com |
Device Dimensions
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00612649213842 [Package] Contains: 00612649213859 Package: [50 Units] In Commercial Distribution |
| GS1 | 00612649213859 [Primary] |
FDA Product Code
| CAI | Circuit, breathing (w connector, adaptor, y piece) |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | false |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2019-11-27 |
| Device Publish Date | 2019-04-17 |
On-Brand Devices [UNIVERSAL FLEX2®]
| 00612649213842 | UNIVERSAL FLEX2 CIRCUIT |
| 00612649213828 | UNIVERSAL FLEX2 CIRCUIT |
| 00612649215365 | UNIVERSAL FLEX2 CIRCUIT |
| 00612649215341 | UNIVERSAL FLEX2 CIRCUIT |
| 00612649215280 | UNIVERSAL FLEX2 CIRCUIT |
| 00612649215266 | UNIVERSAL FLEX2 CIRCUIT |
| 00612649215303 | UNIVERSAL FLEX2 CIRCUIT |
| 00612649163789 | UNIVERSAL FLEX2 CIRCUIT |
Trademark Results [UNIVERSAL FLEX2]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 UNIVERSAL FLEX2 76588618 3088083 Live/Registered |
King Systems Corporation 2004-04-26 |
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