Primary Device ID | 07613327504453 |
NIH Device Record Key | 257ec58d-2e61-4894-9307-2c7bed8d7ac0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Power-LOAD |
Version Model Number | 639005550003 |
Catalog Number | 639005550003 |
Company DUNS | 078470558 |
Company Name | STRYKER CORPORATION |
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 | false |
Serial Number | true |
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 |
Handling Environment Temperature | Between -30 Degrees Fahrenheit and 130 Degrees Fahrenheit |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07613327504453 [Primary] |
FPO | STRETCHER, WHEELED |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-12-25 |
Device Publish Date | 2019-12-17 |
07613327394740 | 6390 |
07613327261523 | 6390 |
07613327504453 | 639005550003 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
POWER-LOAD 77504518 4210289 Live/Registered |
Stryker Corporation 2008-06-20 |