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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
Suction system bottle/canister sealing set FDA UDI
Device Name
CUSTOM SURGICAL KIT LIPO CANISTER 2000CC FDA UDI
Model / Reference
525-073 FDA UDI
Description
CUSTOM SURGICAL KIT LIPO CANISTER 2000CC FDA UDI

Identifiers

Primary DI / UDI-DI
M7525250730 FDA UDI
FDA Product Code
KDQ FDA UDI
GMDN Term
Suction system bottle/canister sealing set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 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

No

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: Suction system bottle/canister sealing set

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

Similar devices

Also classified as Suction system bottle/canister sealing set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 96810583-d034-4eec-818c-0fa2d1f553c6 34 fields · synced May 30, 2026