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Stradis Medical, LLC.

FDA UDI

by Stradis Medical, Llc

Identity

Trade Name
Stradis Medical, LLC. FDA UDI
Generic Name
General-purpose syringe/needle FDA UDI
Device Name
ANA Kit FDA UDI
Model / Reference
999281467 FDA UDI
Description
ANA Kit FDA UDI

Identifiers

Primary DI / UDI-DI
M7529992814671 FDA UDI
GMDN Term
General-purpose syringe/needle FDA UDI

Classification

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: General-purpose syringe/needle

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

Similar devices

Also classified as General-purpose syringe/needle.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 99b1dd64-4c7f-4fb4-a39b-fe03f714ae25 34 fields · synced May 29, 2026