TONOPORT BP Single-Use Cuff for Adults, Extra-large

FDA UDI

Class II (US FDA UDI)

by PAR Medizintechnik GmbH & Co. Kommanditgesellschaft

Identity

Trade Name: TONOPORT BP Single-Use Cuff for Adults, Extra-large FDA UDI
Generic Name: Blood pressure cuff, single-use FDA UDI
Model / Reference: 2001589-235 FDA UDI

Identifiers

Primary DI / UDI-DI: 04260671372233 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

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

Yes

FDA UDI

Dimensions & Sizes

Size: Length — 640 Millimeter FDA UDI
Width — 175 Millimeter FDA UDI

Category: Blood pressure cuff, single-use

TONOPORT BP Single-Use Cuff for Adults, Extra-large by PAR Medizintechnik GmbH & Co. Kommanditgesellschaft — Class II — FDA UDI — listed in FDA GUDID

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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 II	Pending data

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Manufacturer

Manufacturer: PAR Medizintechnik GmbH & Co. Kommanditgesellschaft

Sources (1)

FDA UDI e31029d6-ac63-4221-91c8-83016422b0b5 35 fields · synced May 30, 2026