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Stradis Healthcare

FDA UDI

Class I (US FDA UDI)

by Stradis Medical, Llc

Identity

Trade Name
STRADIS HEALTHCARE FDA UDI
Generic Name
Blood collection tube holder/needle FDA UDI
Model / Reference
ZZ-0703 FDA UDI

Identifiers

Primary DI / UDI-DI
M752ZZ07030 FDA UDI
FDA Product Code
FHQ FDA UDI
GMDN Term
Blood collection tube holder/needle FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.4730 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

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

Category: Blood collection tube holder/needle

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

Similar devices

Also classified as Blood collection tube holder/needle.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a46db308-3690-4a44-9821-057025f6f270 33 fields · synced Jun 8, 2026