Primary Device ID | 09421901970598 |
NIH Device Record Key | 7f2c3108-6dc5-4aa7-8dcd-1d92a2e80a9f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Suction Tubes Bent - 22 Gauge Non-Sterile |
Version Model Number | NZ5253Bent |
Company DUNS | 592534619 |
Company Name | ADEPT MEDICAL LIMITED |
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 | 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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 09421901970598 [Primary] |
JZF | Tube, Ear Suction |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-04-29 |
Device Publish Date | 2024-04-19 |
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