Primary Device ID | 00048503896560 |
NIH Device Record Key | c070340f-e920-4f6b-9555-c1e93fe43f2a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Truform® |
Version Model Number | 8865CH-XL |
Company DUNS | 004247383 |
Company Name | SURGICAL APPLIANCE INDUSTRIES, 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 | true |
Lot Batch | true |
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 | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00048503896560 [Primary] |
DWL | Stocking, Medical Support (To Prevent Pooling Of Blood In Legs) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2019-10-07 |
Device Publish Date | 2018-03-19 |