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Lippman Nucleus Spatula

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
LIPPMAN NUCLEUS SPATULA FDA UDI
Generic Name
Ophthalmic surgical probe, reusable FDA UDI
Device Name
LIPPMAN NUCLEUS SPATULA BLUNT FORKED ROUND CURVED ANGLED TIP STAINLESS STEEL FDA UDI
Model / Reference
12-2730 FDA UDI
Description
LIPPMAN NUCLEUS SPATULA BLUNT FORKED ROUND CURVED ANGLED TIP STAINLESS STEEL FDA UDI

Identifiers

Catalog Number
12-2730 FDA UDI
Primary DI / UDI-DI
00192896013353 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
Outer Diameter — 0.5 Millimeter FDA UDI

Category: Ophthalmic surgical probe, reusable

Lippman Nucleus Spatula 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 bb2b55e4-ddc4-40e4-85fc-b93c982e6d52 36 fields · synced Jun 8, 2026