← Back to catalogue

Medline

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Blood pressure cuff, single-use FDA UDI
Device Name
DBD-CUFF,BP,DISP,2 TUBE,SM ADULT LONG FDA UDI
Model / Reference
MDS9712DML FDA UDI
Description
DBD-CUFF,BP,DISP,2 TUBE,SM ADULT LONG FDA UDI

Identifiers

Catalog Number
MDS9712DML FDA UDI
Primary DI / UDI-DI
10888277190757 FDA UDI
510(k) Number
K071244 FDA UDI
K161035 FDA UDI
FDA Product Code
DXQ FDA UDI
GMDN Term
Blood pressure cuff, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1120 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

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: Blood pressure cuff, single-use

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

Similar devices

Also classified as Blood pressure cuff, single-use.

Cleared under the same submission

K071244 also covers:

K161035 also covers:

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 603c574f-1864-4d26-bdfe-5f62d8541797 36 fields · synced May 30, 2026