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RespArray NIBP Cuff

FDA UDI

Class II (US FDA UDI)

by Edan Instruments, Inc.

Identity

Trade Name
RespArray NIBP Cuff FDA UDI
Generic Name
Blood pressure cuff, reusable FDA UDI
Model / Reference
01.57.472318 FDA UDI

Identifiers

Primary DI / UDI-DI
06944413824812 FDA UDI
510(k) Number
K220308 FDA UDI
K240320 FDA UDI
FDA Product Code
DXQ FDA UDI
GMDN Term
Blood pressure cuff, reusable 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

No

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Blood pressure cuff, reusable

RespArray NIBP Cuff by Edan Instruments, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood pressure cuff, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f6c350da-a9ca-4ba2-8e98-d827ef636f3d 33 fields · synced Jun 1, 2026