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Stradis Healthcare

FDA UDI

Class II (US FDA UDI)

by Stradis Medical, Llc

Identity

Trade Name
STRADIS HEALTHCARE FDA UDI
Generic Name
Lacrimal tube FDA UDI
Model / Reference
TP-SILICONE FDA UDI

Identifiers

Primary DI / UDI-DI
M752TPSILICONE0 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Lacrimal tube

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

Similar devices

Also classified as Lacrimal tube.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2a486236-6c95-4a01-9ad6-c0e4231532ee 32 fields · synced May 30, 2026