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ClampEase U-View Disc

FDA UDI

Class II (US FDA UDI)

by Semler Technologies, Inc.

Identity

Trade Name
ClampEase U-View Disc FDA UDI
Generic Name
Femoral artery compression system, manual, single-use FDA UDI
Device Name
The ClampEase U-View U-OS003 Disc is a femoral artery medium oval slotted pressure disc with a TAPER attach. FDA UDI
Model / Reference
U-OS003 FDA UDI
Description
The ClampEase U-View U-OS003 Disc is a femoral artery medium oval slotted pressure disc with a TAPER attach. FDA UDI

Identifiers

Catalog Number
150-2012-50a FDA UDI
Primary DI / UDI-DI
10815614021061 FDA UDI
510(k) Number
K964663 FDA UDI
FDA Product Code
DXC FDA UDI
GMDN Term
Femoral artery compression system, manual, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4450 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Femoral artery compression system, manual, single-use

ClampEase U-View Disc by Semler Technologies, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Femoral artery compression system, manual, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 59b77e73-c737-4bf2-83ac-0abc29f42c46 35 fields · synced Jun 8, 2026