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Mabis

FDA UDI

Class II (US FDA UDI)

by Dms Holdings, Inc.,

Identity

Trade Name
MABIS FDA UDI
Generic Name
Blood pressure cuff, reusable FDA UDI
Device Name
NYLON CUFF W/1-TUBE BLADDER BLUE ADULT FDA UDI
Model / Reference
05-269-011 FDA UDI
Description
NYLON CUFF W/1-TUBE BLADDER BLUE ADULT FDA UDI

Identifiers

Catalog Number
05-269-011 FDA UDI
Primary DI / UDI-DI
00767056690110 FDA UDI
FDA Product Code
DXN FDA UDI
GMDN Term
Blood pressure cuff, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1130 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

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, reusable

Mabis by Dms Holdings, Inc., — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood pressure cuff, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dms Holdings, Inc.,

Sources (1)

  • FDA UDI 97e1edf5-3e59-496b-9d3d-29a309b92bdd 34 fields · synced Jun 1, 2026