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Mabis

FDA UDI

Class II (US FDA UDI)

by Dms Holdings, Inc.,

Identity

Trade Name
MABIS FDA UDI
Generic Name
Aneroid manual sphygmomanometer FDA UDI
Device Name
MATCH MATES SPHYG W/DUAL HEAD STETHOSCOPE BURGUNDY ADULT FDA UDI
Model / Reference
01-260-071 FDA UDI
Description
MATCH MATES SPHYG W/DUAL HEAD STETHOSCOPE BURGUNDY ADULT FDA UDI

Identifiers

Catalog Number
01-260-071 FDA UDI
Primary DI / UDI-DI
00767056260078 FDA UDI
510(k) Number
K082542 FDA UDI
FDA Product Code
DXQ FDA UDI
GMDN Term
Aneroid manual sphygmomanometer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1120 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

Yes

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

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

Cleared under the same submission

K082542 also covers:

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 37393572-5bdd-46b3-9c15-11557f558029 36 fields · synced May 30, 2026