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Model 30™ Tip and Membrane Assembly for Pneumatonometer

FDA UDI

Class II (US FDA UDI)

by Reichert Inc.

Identity

Trade Name
Model 30™ Tip and Membrane Assembly for Pneumatonometer FDA UDI
Generic Name
Ophthalmic tonometer, line-powered FDA UDI
Device Name
One (1) replacement tip and membrane assembly that attaches to the Model 30 Pneumatonometer probe. Probe tip touches a patient's cornea during the measurement. FDA UDI
Model / Reference
230676 FDA UDI
Description
One (1) replacement tip and membrane assembly that attaches to the Model 30 Pneumatonometer probe. Probe tip touches a patient's cornea during the measurement. FDA UDI

Identifiers

Primary DI / UDI-DI
00812559012164 FDA UDI
FDA Product Code
HKX FDA UDI
GMDN Term
Ophthalmic tonometer, line-powered 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Ophthalmic tonometer, line-powered

Model 30™ Tip and Membrane Assembly for Pneumatonometer by Reichert Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic tonometer, line-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Reichert Inc.

Sources (1)

  • FDA UDI fa323401-f0c9-46ff-ad7c-cd910f8fcef0 34 fields · synced May 30, 2026