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MST Scleral IOL Fixation

FDA UDI

Class I (US FDA UDI)

by Microsurgical Technology, Inc.

Identity

Trade Name
MST Scleral IOL Fixation FDA UDI
Generic Name
Ophthalmic surgical procedure kit, non-medicated, single-use FDA UDI
Device Name
Scleral IOL Fixation Solutions Pack FDA UDI
Model / Reference
SFP-1001 FDA UDI
Description
Scleral IOL Fixation Solutions Pack FDA UDI

Identifiers

Catalog Number
SFP-1001 FDA UDI
Primary DI / UDI-DI
00844685008636 FDA UDI
FDA Product Code
HNM FDA UDI
HMR FDA UDI
GMDN Term
Ophthalmic surgical procedure kit, non-medicated, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4350 FDA UDI
886.4570 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Ophthalmic surgical procedure kit, non-medicated, single-use

MST Scleral IOL Fixation by Microsurgical Technology, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic surgical procedure kit, non-medicated, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Microsurgical Technology, Inc.

Sources (1)

  • FDA UDI ec748c99-0903-4f66-b4fc-ef7c25c3c867 34 fields · synced May 30, 2026