Medline

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name: Medline FDA UDI
Generic Name: Body-surface pressure mapping system FDA UDI
Device Name: 45 DAY BED SENSOR PAD FOR MDT8201 FDA UDI
Model / Reference: MDT82145B6 FDA UDI
Description: 45 DAY BED SENSOR PAD FOR MDT8201 FDA UDI

Identifiers

Catalog Number: MDT82145B6 FDA UDI
Primary DI / UDI-DI: 10888277328990 FDA UDI
FDA Product Code: KMI FDA UDI
GMDN Term: Body-surface pressure mapping system FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 880.2400 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Body-surface pressure mapping system

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Medline Industries, Inc.

Sources (1)

FDA UDI 319dd9d0-7a17-453b-a7ad-74fbbdd58af0 35 fields · synced Jun 6, 2026