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Walcott Rx Products

FDA UDI

Class I (US FDA UDI)

by Psi/Eye-Ko, Inc.

Identity

Trade Name
Walcott Rx Products FDA UDI
Generic Name
Lacrimal procedural cannula FDA UDI
Device Name
Lacrimal Cannula 19g, tapered to 23g, straight FDA UDI
Model / Reference
Rx8000S FDA UDI
Description
Lacrimal Cannula 19g, tapered to 23g, straight FDA UDI

Identifiers

Primary DI / UDI-DI
00840516134963 FDA UDI
FDA Product Code
HMX FDA UDI
GMDN Term
Lacrimal procedural cannula FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4350 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Radiation Sterilization FDA UDI

Category: Lacrimal procedural cannula

Walcott Rx Products by Psi/Eye-Ko, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Lacrimal procedural cannula.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Psi/Eye-Ko, Inc.

Sources (1)

  • FDA UDI 71206b72-a9c8-4f2c-aa16-a56349bec638 34 fields · synced Jun 8, 2026