Hokanson

FDA UDI

Class II (US FDA UDI)

by D. E. Hokanson, Inc.

Identity

Trade Name: Hokanson FDA UDI
Generic Name: Blood pressure cuff, single-use FDA UDI
Device Name: Natus labeled 2.5 cm disposable digit vascular cuff FDA UDI
Model / Reference: 03763 FDA UDI
Description: Natus labeled 2.5 cm disposable digit vascular cuff FDA UDI

Identifiers

Catalog Number: 03763 FDA UDI
Primary DI / UDI-DI: 00817065021495 FDA UDI
510(k) Number: K932851 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

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

Yes

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

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size: Width — 2.5 Centimeter FDA UDI

Category: Blood pressure cuff, single-use

Hokanson by D. E. Hokanson, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

K932851 also covers:

Hokanson — D. E. Hokanson, Inc.
Hokanson — D. E. Hokanson, Inc.

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 II	Pending data

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Manufacturer

Manufacturer: D. E. Hokanson, Inc.

Sources (1)

FDA UDI cf9c5c4f-c967-4f1b-81b5-e9550989d95c 37 fields · synced Jun 8, 2026