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SchureMed

FDA UDI

Class I (US FDA UDI)

by Schuerch Corporation

Identity

Trade Name
SchureMed FDA UDI
Generic Name
Frame/rail/pole device holder FDA UDI
Device Name
Safety Draw, IV Pole Mount FDA UDI
Model / Reference
800-0059 FDA UDI
Description
Safety Draw, IV Pole Mount FDA UDI

Identifiers

Primary DI / UDI-DI
00810014601595 FDA UDI
FDA Product Code
FWZ FDA UDI
GMDN Term
Frame/rail/pole device holder 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Frame/rail/pole device holder

SchureMed by Schuerch Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Frame/rail/pole device holder.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a02908c6-3edc-461c-8a97-f40ba028e4f0 34 fields · synced Jun 8, 2026