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Medline

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Laparoscope system, reusable FDA UDI
Device Name
LAPAROSCOPE 5MM,300MM, 0 DEG FDA UDI
Model / Reference
END700000 FDA UDI
Description
LAPAROSCOPE 5MM,300MM, 0 DEG FDA UDI

Identifiers

Catalog Number
END700000 FDA UDI
Primary DI / UDI-DI
10884389183410 FDA UDI
FDA Product Code
FAJ FDA UDI
GMDN Term
Laparoscope system, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Laparoscope system, reusable

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

Similar devices

Also classified as Laparoscope system, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 413c425a-e12b-4312-807f-73cab0794bf2 35 fields · synced May 30, 2026