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Pascal

FDA UDI

Class II (US FDA UDI)

by SMT Swiss Microtechnology AG

Identity

Trade Name
PASCAL FDA UDI
Generic Name
Ophthalmic tonometer, battery-operated FDA UDI
Device Name
SensorCaps-240 FDA UDI
Model / Reference
Sensorcaps FDA UDI
Description
SensorCaps-240 FDA UDI

Identifiers

Catalog Number
311.701.201 FDA UDI
Primary DI / UDI-DI
07640167751174 FDA UDI
510(k) Number
K032967 FDA UDI
FDA Product Code
HKY FDA UDI
GMDN Term
Ophthalmic tonometer, battery-operated FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.1930 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: Ophthalmic tonometer, battery-operated

Pascal by SMT Swiss Microtechnology AG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic tonometer, battery-operated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI bf6d53bc-7026-428f-b571-00dc0987f577 35 fields · synced May 30, 2026