| Primary Device ID | 00885556900635 |
| NIH Device Record Key | 7d3281c1-d7e3-4788-a64d-74db818c32a9 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | LEGION/GII |
| Version Model Number | 71935915 |
| Catalog Number | 71935915 |
| Company DUNS | 045483575 |
| Company Name | Smith & Nephew, 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 | 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 | true |
| OTC Over-The-Counter | false |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00885556900635 [Primary] |
| HWB | EXTRACTOR |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00885556900635]
Moist Heat or Steam Sterilization
[00885556900635]
Moist Heat or Steam Sterilization
[00885556900635]
Moist Heat or Steam Sterilization
[00885556900635]
Moist Heat or Steam Sterilization
[00885556900635]
Moist Heat or Steam Sterilization
[00885556900635]
Moist Heat or Steam Sterilization
[00885556900635]
Moist Heat or Steam Sterilization
[00885556900635]
Moist Heat or Steam Sterilization
[00885556900635]
Moist Heat or Steam Sterilization
[00885556900635]
Moist Heat or Steam Sterilization
[00885556900635]
Moist Heat or Steam Sterilization
[00885556900635]
Moist Heat or Steam Sterilization
[00885556900635]
Moist Heat or Steam Sterilization
[00885556900635]
Moist Heat or Steam Sterilization
[00885556900635]
Moist Heat or Steam Sterilization
[00885556900635]
Moist Heat or Steam Sterilization
[00885556900635]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-09-18 |
| Device Publish Date | 2024-09-10 |
| 00885556731949 | GII Thinned Spacer Block |
| 00885556900550 | PATELLA CAPTURE ROUND 26MM |
| 00885556900635 | TIBIA REMOVAL TOOL |
| 00885556900628 | PATELLA SECONDARY SCREW CLAMP |
| 00885556900611 | PATELLA CLAMP ATTACHMENT |
| 00885556900604 | PATELLA CAPTURE ROUND/OVAL 41MM |
| 00885556900598 | PATELLA CAPTURE ROUND/OVAL 38MM |
| 00885556900581 | PATELLA CAPTURE ROUND/OVAL 35MM |
| 00885556900574 | PATELLA CAPTURE ROUND/OVAL 32MM |
| 00885556900567 | PATELLA CAPTURE ROUND/OVAL 29MM |