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Setmark

FDA UDI

Class I (US FDA UDI)

by Setmark Inc.

Identity

Trade Name
Setmark FDA UDI
Generic Name
Chair/stool armrest FDA UDI
Device Name
Base for Stool, 5 leg,l 15" -21" height adjustment, - stainless steel, FDA UDI
Model / Reference
DC-102 FDA UDI
Description
Base for Stool, 5 leg,l 15" -21" height adjustment, - stainless steel, FDA UDI

Identifiers

Primary DI / UDI-DI
00854204008320 FDA UDI
FDA Product Code
FZM FDA UDI
GMDN Term
Chair/stool armrest FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4950 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Chair/stool armrest

Setmark by Setmark Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Chair/stool armrest.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Setmark Inc.

Sources (1)

  • FDA UDI fa435c5f-2b93-4077-9466-62f4677608c3 33 fields · synced May 30, 2026