Primary Device ID | D2484522220 |
NIH Device Record Key | 1b80476d-3e65-46d5-bf5e-3db439214baf |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MetaLIFT Regular Removal Instrument Replacement Part |
Version Model Number | 452222 |
Company DUNS | 009277971 |
Company Name | HAGER WORLDWIDE, INC. |
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 | false |
Serial Number | false |
Manufacturing Date | false |
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 |
---|---|
HIBCC | D2484522220 [Primary] |
EIS | REMOVER, CROWN |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-12-15 |
Device Publish Date | 2023-12-07 |
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