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Hcs

FDA UDI

Class II (US FDA UDI)

by Dyad Medical Sourcing, Llc

Identity

Trade Name
HCS FDA UDI
Generic Name
Aneroid manual sphygmomanometer FDA UDI
Device Name
Replacement Cuff & Bladder, Latex Free, Adult FDA UDI
Model / Reference
HCS9022 FDA UDI
Description
Replacement Cuff & Bladder, Latex Free, Adult FDA UDI

Identifiers

Primary DI / UDI-DI
00849027000057 FDA UDI
FDA Product Code
DXN FDA UDI
GMDN Term
Aneroid manual sphygmomanometer 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: Aneroid manual sphygmomanometer

Hcs by Dyad Medical Sourcing, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Aneroid manual sphygmomanometer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 63ca4bfe-07e9-452a-8405-a2a1b1b8af38 33 fields · synced Jun 1, 2026