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Softec Hd Pli

FDA UDI

Class III (US FDA UDI)

by Lenstec Barbados Inc

Identity

Trade Name
SOFTEC HD PLI FDA UDI
Generic Name
Posterior-chamber intraocular lens, pseudophakic FDA UDI
Device Name
IOL - HEMA 6.0/13mm (Pre-loaded) FDA UDI
Model / Reference
SOFHDPLI+28.0D and PLITIP1645 Kit FDA UDI
Description
IOL - HEMA 6.0/13mm (Pre-loaded) FDA UDI

Identifiers

Catalog Number
SOFTEC HD PLI FDA UDI
Primary DI / UDI-DI
00844369002776 FDA UDI
PMA Number
P090022 FDA UDI
FDA Product Code
HQL FDA UDI
GMDN Term
Posterior-chamber intraocular lens, pseudophakic FDA UDI

Classification

Device Class
Class III FDA UDI
Regulation Number
886.3600 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Posterior-chamber intraocular lens, pseudophakic

Softec Hd Pli by Lenstec Barbados Inc — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Posterior-chamber intraocular lens, pseudophakic.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9319a33c-4be9-4974-9ecd-79c4cb8a51ab 38 fields · synced May 30, 2026