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Lsl Healthcare

FDA UDI

Class II (US FDA UDI)

by Lsl Industries, Inc.

Identity

Trade Name
LSL HEALTHCARE FDA UDI
Generic Name
Suture kit, medicated FDA UDI
Device Name
Incision & Drainage Tray FDA UDI
Model / Reference
7642 FDA UDI
Description
Incision & Drainage Tray FDA UDI

Identifiers

Catalog Number
7642 FDA UDI
Primary DI / UDI-DI
00661392008373 FDA UDI
FDA Product Code
OVN FDA UDI
GMDN Term
Suture kit, medicated FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4830 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Suture kit, medicated

Lsl Healthcare by Lsl Industries, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Suture kit, medicated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2b03d017-9e15-47cb-8726-19cbd8d7bce5 34 fields · synced May 30, 2026