Primary Device ID | 00885556768877 |
NIH Device Record Key | 96336d22-6689-4bff-8f6e-fbb091d15e1b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PERILOC |
Version Model Number | E0016721-1 |
Catalog Number | E0016721-1 |
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 | 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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00885556768877 [Primary] |
HRY | PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00885556768877]
Moist Heat or Steam Sterilization
[00885556768877]
Moist Heat or Steam Sterilization
[00885556768877]
Moist Heat or Steam Sterilization
[00885556768877]
Moist Heat or Steam Sterilization
[00885556768877]
Moist Heat or Steam Sterilization
[00885556768877]
Moist Heat or Steam Sterilization
[00885556768877]
Moist Heat or Steam Sterilization
[00885556768877]
Moist Heat or Steam Sterilization
[00885556768877]
Moist Heat or Steam Sterilization
[00885556768877]
Moist Heat or Steam Sterilization
[00885556768877]
Moist Heat or Steam Sterilization
[00885556768877]
Moist Heat or Steam Sterilization
[00885556768877]
Moist Heat or Steam Sterilization
[00885556768877]
Moist Heat or Steam Sterilization
[00885556768877]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-11-07 |
Device Publish Date | 2019-10-30 |
00885556748398 | RIB PERIOSTEAL ELEVATOR |
00885556748381 | BALL SPIKE / PADDLE PELVIC REDUCTION FORCEPS |
00885556748374 | DUAL BALL SPIKE PELVIC REDUCTION FORCEPS |
00885556768884 | T25 SCREWDRIVER ONE PIECE |
00885556768877 | 3.5MM HEX HEAD SCREWDRIVER ONE PIECE |
00885556755501 | BALL SPIKE / PADDLE PELVIC REDUCTION FORCEPS |
00885556809563 | 4.5MM PROXIMAL FEMUR LOCKING PLATE 12 HOLE LEFT |
00885556811092 | PROX FEM LOCKING PLATE 6H LT PROX FEM LOCKING PLATE 6H LT |
00885556889695 | T25 SCREWDRIVER ONE PIECE |
00885556889688 | 3.5MM HEX HEAD SCREWDRIVER ONE PIECE |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PERILOC 79152395 4838779 Live/Registered |
Danspin A/S 2014-05-12 |