← Back to catalogue

Stradis Medical, LLC.

FDA UDI

Class II (US FDA UDI)

by Stradis Medical, Llc

Identity

Trade Name
Stradis Medical, LLC. FDA UDI
Generic Name
Blood collection set, invasive FDA UDI
Device Name
Pen Needle Kit FDA UDI
Model / Reference
511389 FDA UDI
Description
Pen Needle Kit FDA UDI

Identifiers

Primary DI / UDI-DI
M7525113890 FDA UDI
FDA Product Code
PQD FDA UDI
GMDN Term
Blood collection set, invasive FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1675 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

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: Blood collection set, invasive

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

Similar devices

Also classified as Blood collection set, invasive.

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

Sources (1)

  • FDA UDI fc153bc1-e336-4df2-8dba-7ce9956dcbac 34 fields · synced May 30, 2026