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Hu Capsular Polisher

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
Hu Capsular Polisher FDA UDI
Generic Name
Ophthalmic surgical probe, reusable FDA UDI
Device Name
HU Capsular Polisher E0645 Single End Angled With Loop Stainless Steel FDA UDI
Model / Reference
12-2685 FDA UDI
Description
HU Capsular Polisher E0645 Single End Angled With Loop Stainless Steel FDA UDI

Identifiers

Primary DI / UDI-DI
00192896112193 FDA UDI
FDA Product Code
HND FDA UDI
GMDN Term
Ophthalmic surgical probe, reusable FDA UDI

Classification

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

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 5 Inch FDA UDI

Category: Ophthalmic surgical probe, reusable

Hu Capsular Polisher by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic surgical probe, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2d593636-52e9-4ca5-bf70-b8f2edbaf50f 35 fields · synced Jun 8, 2026