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LATITUDE® Communicator with Wand

FDA UDI

Class III (US FDA UDI)

by Boston Scientific

Identity

Trade Name
LATITUDE® Communicator with Wand FDA UDI
Generic Name
Patient monitoring modem FDA UDI
Device Name
LATITUDE ® Communicator with Wand FDA UDI
Model / Reference
6481 FDA UDI
Description
LATITUDE ® Communicator with Wand FDA UDI

Identifiers

Primary DI / UDI-DI
00802526580727 FDA UDI
PMA Number
P910077 FDA UDI
FDA Product Code
LWS FDA UDI
GMDN Term
Patient monitoring modem FDA UDI

Classification

Device Class
Class III 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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Patient monitoring modem

LATITUDE® Communicator with Wand by Boston Scientific — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Patient monitoring modem.

Cleared under the same submission

P910077 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Boston Scientific

Sources (1)

  • FDA UDI b5ef80e7-c3bd-47d9-8cec-65a6f4d352c4 34 fields · synced May 31, 2026