Truform®
GUDID 00048503892357
SURGICAL APPLIANCE INDUSTRIES, INC.
Compression/pressure sock/stocking, single-use| Primary Device ID | 00048503892357 |
| NIH Device Record Key | f0d50d52-e4c9-4f0b-b9ab-df88b832f789 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Truform® |
| Version Model Number | 1923CH-L |
| 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 Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00048503892357 [Primary] |
FDA Product Code
| DWL | Stocking, Medical Support (To Prevent Pooling Of Blood In Legs) |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | false |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-10-07 |
| Device Publish Date | 2017-01-27 |
On-Brand Devices [Truform®]
Trademark Results [Truform]
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