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Medline

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
MEDLINE FDA UDI
Generic Name
Ophthalmic/otologic diagnostic set FDA UDI
Device Name
OPHTHALMOSCOPE,POCKET,2.5V LED,W/POUCH FDA UDI
Model / Reference
MDSLS4LOP FDA UDI
Description
OPHTHALMOSCOPE,POCKET,2.5V LED,W/POUCH FDA UDI

Identifiers

Catalog Number
MDSLS4LOP FDA UDI
Primary DI / UDI-DI
10193489136210 FDA UDI
FDA Product Code
HLJ FDA UDI
GMDN Term
Ophthalmic/otologic diagnostic set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.1570 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Ophthalmic/otologic diagnostic set

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

Similar devices

Also classified as Ophthalmic/otologic diagnostic set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6c20f73f-a991-4d22-a5e7-6658d367da90 36 fields · synced Jun 8, 2026