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Lanzino Forceps Set

FDA UDI

Class I (US FDA UDI)

by Katalyst Surgical, Llc

Identity

Trade Name
Lanzino Forceps Set FDA UDI
Generic Name
General surgical procedure kit, non-medicated, reusable FDA UDI
Device Name
Lanzino Forceps Set FDA UDI
Model / Reference
N3219-SET FDA UDI
Description
Lanzino Forceps Set FDA UDI

Identifiers

Primary DI / UDI-DI
00840096215144 FDA UDI
FDA Product Code
FSM FDA UDI
GMDN Term
General surgical procedure kit, non-medicated, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: General surgical procedure kit, non-medicated, reusable

Lanzino Forceps Set by Katalyst Surgical, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General surgical procedure kit, non-medicated, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Katalyst Surgical, Llc

Sources (1)

  • FDA UDI 28df08e1-a579-4764-a0d4-e597f8d41b24 33 fields · synced Jun 8, 2026