| Primary Device ID | 05030267011315 |
| NIH Device Record Key | d713c73c-ea39-4b0a-8b44-8e6b6553418e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | LUER ELBOW, 7.6MM PORT |
| Version Model Number | 2710000 |
| Company DUNS | 785952607 |
| Company Name | Intersurgical Incorporated |
| 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 | false |
| Device Combination Product | true |
| 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 | 3154512900 |
| support@intersurgicalinc.com | |
| Phone | 3154512900 |
| support@intersurgicalinc.com | |
| Phone | 3154512900 |
| support@intersurgicalinc.com | |
| Phone | 3154512900 |
| support@intersurgicalinc.com | |
| Phone | 3154512900 |
| support@intersurgicalinc.com | |
| Phone | 3154512900 |
| support@intersurgicalinc.com | |
| Phone | 3154512900 |
| support@intersurgicalinc.com | |
| Phone | 3154512900 |
| support@intersurgicalinc.com | |
| Phone | 3154512900 |
| support@intersurgicalinc.com | |
| Phone | 3154512900 |
| support@intersurgicalinc.com | |
| Phone | 3154512900 |
| support@intersurgicalinc.com | |
| Phone | 3154512900 |
| support@intersurgicalinc.com | |
| Phone | 3154512900 |
| support@intersurgicalinc.com | |
| Phone | 3154512900 |
| support@intersurgicalinc.com | |
| Phone | 3154512900 |
| support@intersurgicalinc.com | |
| Phone | 3154512900 |
| support@intersurgicalinc.com | |
| Phone | 3154512900 |
| support@intersurgicalinc.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 05030267011315 [Package] Contains: 05030267064502 Package: [25 Units] In Commercial Distribution |
| GS1 | 05030267064502 [Primary] |
| GS1 | 05030267090037 [Package] Contains: 05030267064502 Package: [100 Units] In Commercial Distribution |
| BZA | Connector, Airway (Extension) |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-06-23 |
| Device Publish Date | 2023-06-15 |
| 05030267011872 - GAS MONITORING LINE, 1.2MM ID, MALE/MALE LUER LOCK, 3M | 2024-11-01 GAS MONITORING LINE, 1.2MM ID, MALE/MALE LUER LOCK, 3M |
| 05030267163571 - INTERSURGICAL ECOLITE™, ADULT, HIGH CONCENTRATION OXYGEN MASK AND TUBE, 2.1M | 2024-10-17 INTERSURGICAL ECOLITE™, ADULT, HIGH CONCENTRATION OXYGEN MASK AND TUBE WITH UNIVERSAL CONNECTOR, 2.1M |
| 05030267163588 - CIRRUS™2 NEBULISER MOUTHPIECE KIT AND TUBE WITH UNIVERSAL CONNECTOR, 2.1M | 2024-10-17 CIRRUS™2 NEBULISER MOUTHPIECE KIT AND TUBE WITH UNIVERSAL CONNECTOR, 2.1M |
| 05030267163618 - CIRRUS2 NEBULISER, ADULT, INTERSURGICAL ECOLITE MASK KIT AND TUBE, 2.1M | 2024-10-17 CIRRUS2 NEBULISER, ADULT, INTERSURGICAL ECOLITE MASK KIT AND TUBE WITH UNIVERSAL CONNECTOR, 2.1M |
| 05030267163595 - CIRRUS2 NEBULISER, PAEDIATRIC INTERSURGICAL ECOLITE MASK KIT AND TUBE, 2.1M | 2024-10-17 CIRRUS2 NEBULISER, PAEDIATRIC INTERSURGICAL ECOLITE MASK KIT AND TUBE WITH UNIVERSAL CONNECTOR, 2.1M |
| 05030267167142 - CLEARLITE™ AIR, ANAESTHETIC FACE MASK, SIZE 4, ADULT, GREEN SEAL, 22F | 2024-10-17 CLEARLITE™ AIR, ANAESTHETIC FACE MASK, SIZE 4, ADULT, GREEN SEAL, 22F |
| 05030267167166 - CLEARLITE™ AIR, ANAESTHETIC FACE MASK SIZE 4 ADULT GREEN SEAL NO HOOK RING 22F | 2024-10-17 CLEARLITE™ AIR, ANAESTHETIC FACE MASK, SIZE 4, ADULT, GREEN SEAL, NO HOOK RING, 22F |
| 05030267040865 - 22MM SMOOTHBORE REUSABLE EXHALATION VALVE BREATHING SYSTEM. 1.6M | 2024-09-24 22MM SMOOTHBORE REUSABLE EXHALATION VALVE BREATHING SYSTEM. 1.6M |