← Back to catalogue

Disposable Instruments

FDA UDI

Class U (US FDA UDI)

by OASIS Medical, Inc.

Identity

Trade Name
Disposable Instruments FDA UDI
Generic Name
Lacrimal intubation set FDA UDI
Device Name
Lacrimal Irrigation Kit, 3-mL Disposable Syringe and a 25g x 1-1/8", Blunt Disposable Cannula FDA UDI
Model / Reference
4003-IK FDA UDI
Description
Lacrimal Irrigation Kit, 3-mL Disposable Syringe and a 25g x 1-1/8", Blunt Disposable Cannula FDA UDI

Identifiers

Primary DI / UDI-DI
00845819006092 FDA UDI
FDA Product Code
OKS FDA UDI
GMDN Term
Lacrimal intubation set FDA UDI

Classification

Device Class
U 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 intubation set

A comprehensive and user-friendly medical device directory that provides detailed information about the Disposable Instruments, including its features, compliance, and FAQs.

Similar devices

Also classified as Lacrimal intubation set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
OASIS Medical, Inc.

Sources (1)

  • FDA UDI 97c4f076-6b2c-4dbe-97af-604b639a2dd3 34 fields · synced Jul 10, 2026