Primary Device ID | 00732094307351 |
NIH Device Record Key | d3ba84cf-be7c-40a9-9fb0-fe39dbd2bac2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Welch Allyn, Inc. |
Version Model Number | 901145 |
Catalog Number | 419751 |
Company DUNS | 198227881 |
Company Name | WELCH ALLYN, INC. |
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 | 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 | 00732094307351 [Primary] |
MHX | MONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR ALARMS) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-10-31 |
Device Publish Date | 2019-10-23 |
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00732094222579 | NOVAPLUS RAW CUFF SOFT ADULT |
00732094222562 | NOVAPLUS RAW CUFF SOFT SMALL ADULT |
00732094222555 | NOVAPLUS RAW CUFF SOFT CHILD |
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00732094128840 | CUFF TL REUSE 2 PC THIGH 1TUBE ML |
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00732094010237 | CUFF TL REUSE 2 PC LG ADULT 1TUBE ML |
00732094128765 | CUFF TL REUSE 2 PC LG AD LONG 1TB LL |
00732094128734 | CUFF TL REUSE 2 PC LG AD LONG 1TB MQ |
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00732094010169 | CUFF TL REUSE 2 PC ADULT 1TUBE LL |
00732094128703 | CUFF TL REUSE 2 PC ADULT 1TUBE MQ |
00732094128666 | CUFF TL REUSE 2 PC ADULT LONG 1TB LL |
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00732094010077 | CUFF TL REUSE 2 PC SM ADULT 1TUBE LL |
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00732094010053 | CUFF TL REUSE 2 PC SM ADULT 1TUBE ML |
00732094010015 | CUFF TL REUSE 2 PC CHILD 1TUBE LL |
00732094009989 | CUFF TL REUSE 2 PC CHILD 1TUBE MQ |
00732094009996 | CUFF TL REUSE 2 PC CHILD 1TUBE ML |