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Medline

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
MEDLINE FDA UDI
Generic Name
Microscope slide hybridization/denaturation incubator IVD FDA UDI
Device Name
COMBO,LARYNG,MAC3,MEDIUM HANDLE FDA UDI
Model / Reference
MDS0180103 FDA UDI
Description
COMBO,LARYNG,MAC3,MEDIUM HANDLE FDA UDI

Identifiers

Catalog Number
MDS0180103 FDA UDI
Primary DI / UDI-DI
10197344135950 FDA UDI
FDA Product Code
CCW FDA UDI
GMDN Term
Microscope slide hybridization/denaturation incubator IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

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

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Microscope slide hybridization/denaturation incubator IVD

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

Similar devices

Also classified as Microscope slide hybridization/denaturation incubator IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medline Industries, Inc.

Sources (1)

  • FDA UDI caceea5e-caf1-4463-a5fb-bd72e319b178 35 fields · synced Jun 8, 2026