← Back to catalogue

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
BLADE,LARYNG,SINGLE USE,ROBERTSHAW0 FDA UDI
Model / Reference
MDS0169100 FDA UDI
Description
BLADE,LARYNG,SINGLE USE,ROBERTSHAW0 FDA UDI

Identifiers

Catalog Number
MDS0169100 FDA UDI
Primary DI / UDI-DI
10197344135882 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Medline Industries, Inc.

Sources (1)

  • FDA UDI 89b3a8e5-e112-43f1-803e-9b6356478a0c 35 fields · synced May 30, 2026