Stradis Medical, LLC.

FDA UDI

Class II (US FDA UDI)

by Stradis Medical, Llc

Identity

Trade Name: Stradis Medical, LLC. FDA UDI
Generic Name: Lacrimal tube FDA UDI
Model / Reference: 680-089 FDA UDI

Identifiers

Primary DI / UDI-DI: M7526800890 FDA UDI
FDA Product Code: MIB FDA UDI
GMDN Term: Lacrimal tube FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 874.3620 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Lacrimal tube

Stradis Medical, LLC. by Stradis Medical, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Stradis Medical, Llc

Sources (1)

FDA UDI f823e61f-1474-4ce8-8e16-fd5e08b80ea1 33 fields · synced May 30, 2026