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WorkMate Claris™

FDA UDI

Class II (US FDA UDI)

by St. Jude Medical, Inc.

Identity

Trade Name
WorkMate Claris™ FDA UDI
Generic Name
Laser printer FDA UDI
Device Name
System Printer FDA UDI
Model / Reference
H701806 FDA UDI
Description
System Printer FDA UDI

Identifiers

Catalog Number
H701806 FDA UDI
Primary DI / UDI-DI
05415067018069 FDA UDI
510(k) Number
K092913 FDA UDI
K210392 FDA UDI
FDA Product Code
JOQ FDA UDI
DQK FDA UDI
GMDN Term
Laser printer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1750 FDA UDI
870.1425 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

Yes

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Laser printer

WorkMate Claris™ by St. Jude Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laser printer.

Cleared under the same submission

K092913 also covers:

K210392 also covers:

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
St. Jude Medical, Inc.

Sources (1)

  • FDA UDI 37b1e262-7327-4729-998d-4bffeccf0821 37 fields · synced Jun 7, 2026