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Tech-Med

FDA UDI

Class II (US FDA UDI)

by Dukal LLC

Identity

Trade Name
Tech-Med FDA UDI
Generic Name
Blood pressure cuff, reusable FDA UDI
Device Name
Manometer, Black FDA UDI
Model / Reference
2911 FDA UDI
Description
Manometer, Black FDA UDI

Identifiers

Catalog Number
2911 FDA UDI
Primary DI / UDI-DI
10665973016976 FDA UDI
510(k) Number
K193259 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

No

FDA UDI

Over-the-Counter

Yes

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, reusable

Tech-Med by Dukal LLC — 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

Manufacturer
Dukal LLC

Sources (1)

  • FDA UDI 5f4198db-660c-4439-8aa0-982f5f182623 36 fields · synced May 30, 2026