Primary Device ID | 00041298405603 |
NIH Device Record Key | 81f1c007-e741-42c8-98ac-b55ada377cd4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | DMI |
Version Model Number | 553-4056-0400 |
Company DUNS | 062028220 |
Company Name | D-M-S HOLDINGS, 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 |
---|---|
GS1 | 00041298405603 [Primary] |
INW | Table, Mechanical |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-08-14 |
Device Publish Date | 2023-08-04 |
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00041298802112 | CUSHION WHEELCHAIR NAVY |
00041298802013 | Polyfoam Wheelchair Cushion Navy |
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10041298080074 | Ring Inflatable Rubber Large |
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