← Back to catalogue

MEDRAD® Veris™ 8600 Vital Signs Monitor

FDA UDI

Class II (US FDA UDI)

by Bayer Medical Care Inc.

Identity

Trade Name
MEDRAD® Veris™ 8600 Vital Signs Monitor FDA UDI
Generic Name
Blood pressure cuff, single-use FDA UDI
Device Name
"Adult Blood Pressure Disposable Cuffs 12-15.5 in (30.5-39.5 cm) (BP CUFF,DISP,30-40CM,VERIS,MC) (85276719)" FDA UDI
Model / Reference
3011543 FDA UDI
Description
"Adult Blood Pressure Disposable Cuffs 12-15.5 in (30.5-39.5 cm) (BP CUFF,DISP,30-40CM,VERIS,MC) (85276719)" FDA UDI

Identifiers

Catalog Number
3011543 FDA UDI
Primary DI / UDI-DI
00616258009513 FDA UDI
510(k) Number
K042569 FDA UDI
FDA Product Code
MWI FDA UDI
GMDN Term
Blood pressure cuff, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2300 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

MEDRAD® Veris™ 8600 Vital Signs Monitor by Bayer Medical Care 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

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

Sources (1)

  • FDA UDI 20229ced-ee9b-4846-9920-3a3a2bae8a08 36 fields · synced Jun 9, 2026