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TS75 Trial Lens

FDA UDI

Class I (US FDA UDI)

by Reichert Inc.

Identity

Trade Name
TS75 Trial Lens FDA UDI
Generic Name
Trial lens set FDA UDI
Model / Reference
15015 FDA UDI

Identifiers

Primary DI / UDI-DI
00812559010566 FDA UDI
FDA Product Code
HPC FDA UDI
GMDN Term
Trial lens set FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.1405 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Trial lens set

TS75 Trial Lens by Reichert Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Trial lens set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Reichert Inc.

Sources (1)

  • FDA UDI 1d01324d-69f3-4da8-9949-5027d51db5d0 32 fields · synced May 30, 2026