Primary Device ID | 00816472020930 |
NIH Device Record Key | e77705f9-7c78-4533-bb37-cb67c8eae620 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Convenience Pack |
Version Model Number | J0004001 |
Company DUNS | 785952607 |
Company Name | Intersurgical Incorporated |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | MR Safe |
Human Cell/Tissue Product | false |
Device Kit | false |
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 | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 315-451-2900 |
support@intersurgicalinc.com | |
Phone | 315-451-2900 |
support@intersurgicalinc.com | |
Phone | 315-451-2900 |
support@intersurgicalinc.com | |
Phone | 315-451-2900 |
support@intersurgicalinc.com | |
Phone | 315-451-2900 |
support@intersurgicalinc.com | |
Phone | 315-451-2900 |
support@intersurgicalinc.com | |
Phone | 315-451-2900 |
support@intersurgicalinc.com | |
Phone | 315-451-2900 |
support@intersurgicalinc.com | |
Phone | 315-451-2900 |
support@intersurgicalinc.com | |
Phone | 315-451-2900 |
support@intersurgicalinc.com | |
Phone | 315-451-2900 |
support@intersurgicalinc.com | |
Phone | 315-451-2900 |
support@intersurgicalinc.com | |
Phone | 315-451-2900 |
support@intersurgicalinc.com | |
Phone | 315-451-2900 |
support@intersurgicalinc.com | |
Phone | 315-451-2900 |
support@intersurgicalinc.com | |
Phone | 315-451-2900 |
support@intersurgicalinc.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00816472020923 [Primary] |
GS1 | 00816472020930 [Package] Contains: 00816472020923 Package: [20 Units] In Commercial Distribution |
OFP | Anesthesia Breathing Circuit Kit (Adult & Pediatric) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-06-21 |
Device Publish Date | 2023-06-13 |
05030267166077 - VENTURI VALVE 24% OXYGEN, BLUE | 2024-04-12 VENTURI VALVE 24% OXYGEN, BLUE |
05030267166145 - VENTURI VALVE 28% OXYGEN, WHITE | 2024-04-12 VENTURI VALVE 28% OXYGEN, WHITE |
05030267166176 - VENTURI VALVE 35% OXYGEN, YELLOW | 2024-04-12 VENTURI VALVE 35% OXYGEN, YELLOW |
05030267166206 - VENTURI VALVE 40% OXYGEN, RED | 2024-04-12 VENTURI VALVE 40% OXYGEN, RED |
05030267166237 - VENTURI VALVE 60% OXYGEN, GREEN | 2024-04-12 VENTURI VALVE 60% OXYGEN, GREEN |
05030267166268 - VENTURI VALVE 50% OXYGEN, PINK | 2024-04-12 VENTURI VALVE 50% OXYGEN, PINK |
05030267166299 - VENTURI VALVE 31% OXYGEN, ORANGE | 2024-04-12 VENTURI VALVE 31% OXYGEN, ORANGE |
05030267011674 - MONITORING LINE 1.8M, MALE - MALE LUER LOCK CONNECTORS | 2024-02-28 MONITORING LINE 1.8M, MALE - MALE LUER LOCK CONNECTORS |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
CONVENIENCE PACK 76302518 not registered Dead/Abandoned |
Choice One Communications, Inc. 2001-08-21 |
CONVENIENCE PACK 73597079 1435144 Dead/Cancelled |
AMERICAN SEED CORPORATION 1986-05-05 |
CONVENIENCE PACK 73506663 1350132 Live/Registered |
SUNBELT MANUFACTURING, INC. 1984-11-01 |