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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
General surgical procedure kit, medicated FDA UDI
Device Name
Custom Medical Tray, Vein FDA UDI
Model / Reference
682-639NL1 FDA UDI
Description
Custom Medical Tray, Vein FDA UDI

Identifiers

Primary DI / UDI-DI
M752682639NL10 FDA UDI
FDA Product Code
OEZ FDA UDI
GMDN Term
General surgical procedure kit, medicated FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1200 FDA UDI
Commercial Distribution
Not 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

Yes

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

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3fe7a258-d39b-4a27-a812-8d2dc9a9ab5d 35 fields · synced Jun 8, 2026