| Primary Device ID | 03596010638298 | 
| NIH Device Record Key | 915f66ca-6524-433b-882c-37cb3216d9a8 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | PERI-LOC System | 
| Version Model Number | 71170522 | 
| Catalog Number | 71170522 | 
| Company DUNS | 109903521 | 
| Company Name | Smith & Nephew, Inc. | 
| Device Count | 1 | 
| DM Exempt | false | 
| Pre-market Exempt | false | 
| 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 | false | 
| 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 | |
| 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 | 03596010638298 [Primary] | 
| HRS | Plate, fixation, bone | 
| Steralize Prior To Use | false | 
| Device Is Sterile | false | 
| Public Version Status | New | 
| Device Record Status | Published | 
| Public Version Number | 1 | 
| Public Version Date | 2022-02-24 | 
| Device Publish Date | 2022-02-16 | 
| 03596010638373 | PERI-LOC L-D FEMUR TEMPLATE RIGHT FOR TITANIUM PLATE | 
| 03596010638359 | PERI-LOC L-P TIBIA TEMPLATE RIGHT FOR TITANIUM PLATE | 
| 03596010638335 | PERI-LOC A-L-D TIBIA TEMPLATE 3H RIGHT FOR TITANIUM PLATE | 
| 03596010638298 | PERI-LOC M-D TIBIA TEMPLATE RIGHT FOR TITANIUM PLATE | 
| 03596010638274 | PERI-LOC PROX HUMERUS TEMPLATE RIGHT FOR TITANIUM PLATE | 
| 03596010638250 | PERI-LOC M-D HUMERUS TEMPLATE RIGHT FOR TITANIUM PLATE | 
| 03596010638243 | PERI-LOC M-D HUMERUS TEMPLATE LEFT FOR TITANIUM PLATE | 
| 03596010638236 | PERI-LOC P-L-D HUMERUS TEMPLATE RIGHT FOR TITANIUM PLATE | 
| 03596010638212 | PERI-LOC L-D HUMERUS TEMPLATE RIGHT FOR TITANIUM PLATE | 
| 03596010638199 | PERI-LOC OLECRANON TEMPLATE RIGHT FOR TITANIUM PLATE | 
| 03596010638151 | PERI-LOC WIDE VDR TEMPLATE RIGHT FOR TITANIUM PLATE | 
| 03596010638137 | PERI-LOC STD VDR TEMPLATE RIGHT FOR TITANIUM PLATE | 
| 03596010638168 | PERI-LOC LAT TIBIA BT TEMPLATE RIGHT FOR TITANIUM PLATE |