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Hopkins Medical Products®

FDA UDI

Class II (US FDA UDI)

by Hopkins Uniform Company

Identity

Trade Name
Hopkins Medical Products® FDA UDI
Generic Name
Pulse oximeter FDA UDI
Device Name
Hopkins Finger Pulse Oximeter FDA UDI
Model / Reference
594017 FDA UDI
Description
Hopkins Finger Pulse Oximeter FDA UDI

Identifiers

Catalog Number
594017 FDA UDI
Primary DI / UDI-DI
00817643021428 FDA UDI
FDA Product Code
DQA FDA UDI
GMDN Term
Pulse oximeter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2700 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

Yes

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Pulse oximeter

Hopkins Medical Products® by Hopkins Uniform Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pulse oximeter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d79aa55a-7554-4498-bcee-c8c09e66b976 35 fields · synced Jun 1, 2026