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Stradis

FDA UDI

Class I (US FDA UDI)

by Stradis Medical, Llc

Identity

Trade Name
STRADIS FDA UDI
Generic Name
General surgical procedure kit, medicated FDA UDI
Device Name
CUSTOM DENTAL KIT MINOR ORAL SURGERY PACK FDA UDI
Model / Reference
41022NMP FDA UDI
Description
CUSTOM DENTAL KIT MINOR ORAL SURGERY PACK FDA UDI

Identifiers

Primary DI / UDI-DI
M752D466237R10 FDA UDI
FDA Product Code
PWL FDA UDI
GMDN Term
General surgical procedure kit, medicated FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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

Yes

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

Yes

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: General surgical procedure kit, medicated

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

Similar devices

Also classified as General surgical procedure kit, medicated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 75aa8612-d902-4c43-b458-6cf3017b4f78 34 fields · synced May 31, 2026