Primary Device ID | 07332834001162 |
NIH Device Record Key | b707e32a-6e17-4908-aa37-26b9e01ebc57 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PF 6051-M Pressure Accessory Kit Metal Bayonet |
Version Model Number | PF 6051-M |
Catalog Number | 93-00325 |
Company DUNS | 354765570 |
Company Name | Perimed AB |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | true |
Device Combination Product | false |
Single Use | false |
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 | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07332834001162 [Primary] |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-12-23 |
Device Publish Date | 2024-12-13 |
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