Primary Device ID | 00732094175165 |
NIH Device Record Key | 8cbbcd2f-e290-402a-a5ae-47e657cfd003 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Welch Allyn, Inc. |
Version Model Number | 901025 |
Catalog Number | 42001 |
Company DUNS | 198227881 |
Company Name | WELCH ALLYN, 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 | true |
Serial Number | true |
Manufacturing Date | false |
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 | 00732094175165 [Primary] |
HJN | Transilluminator, battery-powered |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-01-24 |
Device Publish Date | 2020-01-16 |
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00732094010015 | CUFF TL REUSE 2 PC CHILD 1TUBE LL |
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