← Back to catalogue

Setmark Inc.

FDA UDI

Class I (US FDA UDI)

by Setmark Inc.

Identity

Trade Name
Setmark Inc. FDA UDI
Generic Name
General-purpose stool/chair FDA UDI
Model / Reference
DC-108 FDA UDI

Identifiers

Primary DI / UDI-DI
00854204008603 FDA UDI
FDA Product Code
FZM FDA UDI
GMDN Term
General-purpose stool/chair 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: General-purpose stool/chair

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

Similar devices

Also classified as General-purpose stool/chair.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Setmark Inc.

Sources (1)

  • FDA UDI 92c42f8e-a0b9-48b6-ba96-493afe9fa78d 32 fields · synced May 30, 2026