UNIVERSAL FLEX2® KNDF3115-6121Z
GUDID 00612649215266
UNIVERSAL FLEX2 CIRCUIT
King Systems Corporation
Anaesthesia breathing circuit, single-use| Primary Device ID | 00612649215266 |
| NIH Device Record Key | 54b11dc0-60a9-41d5-ac49-d5b31516715e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | UNIVERSAL FLEX2® |
| Version Model Number | KNDF3115-6121Z |
| Catalog Number | KNDF3115-6121Z |
| 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 | true |
| 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
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 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 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 | 00612649215266 [Package] Contains: 00612649215273 Package: [40 Units] In Commercial Distribution |
| GS1 | 00612649215273 [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 | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-06-14 |
| Device Publish Date | 2021-06-04 |
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 |
| 00612649217086 | UNIVERSAL FLEX2 CIRCUIT |
| 00612649217062 | UNIVERSAL FLEX2 CIRCUIT |
| 00612649217048 | UNIVERSAL FLEX2 CIRCUIT |
| 00612649217024 | UNIVERSAL FLEX2 CIRCUIT |
| 00612649217000 | UNIVERSAL FLEX2 CIRCUIT |
| 00612649216942 | 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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