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Laschal Surgical

FDA UDI

Class I (US FDA UDI)

by LASCHAL SURGICAL Instruments, LLC

Identity

Trade Name
Laschal Surgical FDA UDI
Generic Name
Assistive scissors FDA UDI
Device Name
La-3B And La-4C FDA UDI
Model / Reference
1 FDA UDI
Description
La-3B And La-4C FDA UDI

Identifiers

Catalog Number
LA-3B/4C-SET FDA UDI
Primary DI / UDI-DI
B659LA3B4CSET0 FDA UDI
FDA Product Code
LRW FDA UDI
GMDN Term
Assistive scissors 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

No

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Assistive scissors

Laschal Surgical by LASCHAL SURGICAL Instruments, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Assistive scissors.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
LASCHAL SURGICAL Instruments, LLC

Sources (1)

  • FDA UDI 24f6dd9b-0fc5-41e9-8678-2fc6968e946e 34 fields · synced May 30, 2026