← Back to catalogue

SmartStack

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref R100P49-001Model Smart Stack Premium Single

by Maxtec, Inc.

Identity

Trade Name
Smart Stack Equipment Stand EUDAMED
SmartStack FDA UDI
Generic Name
Freestanding/bed-attached intravenous pole FDA UDI
Device Name
Smart Stack IV Pole Stand & Smart Stack Equipment Stand EUDAMED
SMART STACK PREMIUM STAND SINGLE PACK FDA UDI
Model / Reference
R100P49-001 EUDAMEDFDA UDI
Smart Stack Premium Single EUDAMED
Description
SMART STACK PREMIUM STAND SINGLE PACK FDA UDI

Identifiers

Primary DI / UDI-DI
00817770021124 EUDAMEDFDA UDI
Basic UDI-DI
081777002Smartstack68 EUDAMED
Direct Marketing DI
00817770021124 EUDAMED
FDA Product Code
FOX FDA UDI
EMDN Code
V0899 MEDICAL SUPPORT EQUIPMENT - OTHER EUDAMED
GMDN Term
Freestanding/bed-attached intravenous pole FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
880.6990 FDA UDI
Market of Registration
Netherlands EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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

No

FDA UDI

Category: Freestanding/bed-attached intravenous pole

SmartStack by Maxtec, Inc. — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Freestanding/bed-attached intravenous pole.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Maxtec, Inc.

Sources (2)

  • FDA UDI 2d739fdf-dbcf-4d6d-9edc-22f2024555a5 33 fields · synced Jul 12, 2026
  • EUDAMED 095acc17-e32a-41e1-8150-1f508f1869b0 61 fields · synced Jul 12, 2026