← Back to catalogue

BPMS Evolution

FDA UDI

Class I (US FDA UDI)

by Tekscan, Inc.

Identity

Trade Name
BPMS Evolution FDA UDI
Generic Name
Body-surface pressure mapping system FDA UDI
Device Name
Includes 1 Evolution Handle, BPMS Clinical Software CD with Sensor Map corresponding to Sensor 5330, Help File and PDF of System Manual, (1) 5330 Sensor, System Carrying Case, Sensor Carrying Case, and 1 Web-Based Training Session (USA Only) FDA UDI
Model / Reference
BPMS 1 System (5330 Sensors) FDA UDI
Description
Includes 1 Evolution Handle, BPMS Clinical Software CD with Sensor Map corresponding to Sensor 5330, Help File and PDF of System Manual, (1) 5330 Sensor, System Carrying Case, Sensor Carrying Case, and 1 Web-Based Training Session (USA Only) FDA UDI

Identifiers

Catalog Number
BCE5330-1 FDA UDI
Primary DI / UDI-DI
B970BCE533010 FDA UDI
FDA Product Code
JFC FDA UDI
GMDN Term
Body-surface pressure mapping system FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.1600 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Body-surface pressure mapping system

BPMS Evolution by Tekscan, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Body-surface pressure mapping system.

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
Tekscan, Inc.

Sources (1)

  • FDA UDI d4d7f9c4-98c3-4464-9bed-5fcf50cd912b 34 fields · synced May 31, 2026