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Sphygmomanometer

FDA UDI

Class II (US FDA UDI)

by Dynarex Corp.

Identity

Trade Name
Sphygmomanometer FDA UDI
Generic Name
Aneroid manual sphygmomanometer FDA UDI
Model / Reference
7105 FDA UDI

Identifiers

Primary DI / UDI-DI
00616784710518 FDA UDI
510(k) Number
K092245 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
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: Aneroid manual sphygmomanometer

Sphygmomanometer by Dynarex Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Aneroid manual sphygmomanometer.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dynarex Corp.

Sources (1)

  • FDA UDI 836b8527-3676-499a-bb98-9791e2438336 33 fields · synced May 31, 2026