Truform®
GUDID 00048503301231
SURGICAL APPLIANCE INDUSTRIES, INC.
Compression/pressure sock/stocking, single-use| Primary Device ID | 00048503301231 |
| NIH Device Record Key | 95e0951c-861b-4e46-b772-9f7c576fb8e7 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Truform® |
| Version Model Number | NV4468CH-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 | 00048503301231 [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 | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-04-20 |
| Device Publish Date | 2022-04-12 |
On-Brand Devices [Truform®]
Trademark Results [Truform]
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.