Technical Specifications

As our Pre-Loaded Injector (PLI) uses the Softec HD Intraocular lens, please visit the Softec HD Technical Specifications page for more information. However, please note that the diopter range for our PLI is only available in the range below:

Diopter Range:

+10.0 to +27.0

Instructions For Use

PKI08 Softec Series PLI
File Size:	4516 kb
File Type:	pdf

Download File

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Lenstec, Inc.
1765 Commerce Ave. N.
St. Petersburg, FL 33716 USA
Tel: +1 727-571-2272
Fax: +1 727-571-1792

U.S. CUSTOMER SERVICE:
TEL: 1-866-536-7832
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LENSTEC UK

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LENSTEC HOUSE
UNIT 8, MARINER House
CALDER PARK
WAKEFIELD
West Yorkshire wf4 3fl
ENGLAND
TEL: +44 (0)1924 382 678
FAX:+44 (0)1924 850 454

EUROPEAN REGIONAL OFFICE

TRENCIANSKA 47
821 09 BRATISLAVA
SLOVAK REPUBLIC

TEL: 00421905798760

INDICATION
The Lenstec Softec Aspheric Posterior Chamber Intraocular Lens is intended for the replacement of the human crystalline lens following phacoemulsification cataract removal in adults over the age of 21. The lens is indicated for capsular bag placement.
Please note that not all intraocular lenses are available in all countries. Only the SoftecHD, SoftecHDO, SoftecHDM, SoftecI and ClearView 3 intraocular lenses are FDA approved.
CAUTION: Federal (U.S.) law restricts some of these devices to the sale by or on the order of a physician.
Lenstec, Inc. is an ISO 13485 company manufacturing CE Marked Products with additional registrations of several countries.
DUNS: 807554100
© 2021 Lenstec, Inc. All Rights Reserved. Lenstec, Softec, Softec HD, Tetraflex, SBL-3, and the Softec HD logo are registered trademarks of Lenstec, Inc.