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Alcon Grieshaber

FDA UDI

Class II (US FDA UDI)

by Alcon Laboratories, Inc.

Identity

Trade Name
Alcon Grieshaber FDA UDI
Generic Name
Anterior/posterior segment scissors, single-use FDA UDI
Device Name
Advanced DSP Tip MPC Vertical Scissors, 20G FDA UDI
Model / Reference
720.26 FDA UDI
Description
Advanced DSP Tip MPC Vertical Scissors, 20G FDA UDI

Identifiers

Primary DI / UDI-DI
07612717071100 FDA UDI
FDA Product Code
HQE FDA UDI
HQC FDA UDI
GMDN Term
Anterior/posterior segment scissors, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.4150 FDA UDI
886.4670 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

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Needle Gauge — 20 Gauge FDA UDI

Category: Anterior/posterior segment scissors, single-use

Alcon Grieshaber by Alcon Laboratories, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Anterior/posterior segment scissors, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Alcon Laboratories, Inc.

Sources (1)

  • FDA UDI 90b7e384-8f63-42cd-a17a-7f51e412d3b3 35 fields · synced May 30, 2026