Primary Device ID | 00816472020558 |
NIH Device Record Key | 0cc9c971-666c-4222-9772-9883d146f47a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Breathing Circuit |
Version Model Number | A0066000 |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00816472020541 [Primary] |
GS1 | 00816472020558 [Package] Contains: 00816472020541 Package: [15 Units] In Commercial Distribution |
OFP | Anesthesia Breathing Circuit Kit (Adult & Pediatric) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2025-02-11 |
Device Publish Date | 2023-01-12 |
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