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Safe-T-Centesis

FDA UDI

Class II (US FDA UDI)

by Carefusion 2200, Inc

Identity

Trade Name
Safe-T-Centesis FDA UDI
Generic Name
Aspiration tray, single-use FDA UDI
Device Name
Safe-T-Centesis PLUS 8 Fr Catheter Drainage Tray FDA UDI
Model / Reference
PIG1280TSP FDA UDI
Description
Safe-T-Centesis PLUS 8 Fr Catheter Drainage Tray FDA UDI

Identifiers

Catalog Number
PIG1280TSP FDA UDI
Primary DI / UDI-DI
10885403108426 FDA UDI
FDA Product Code
PXI FDA UDI
GMDN Term
Aspiration tray, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5570 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

Yes

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: Aspiration tray, single-use

Safe-T-Centesis by Carefusion 2200, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Aspiration tray, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI dfcc7443-051b-41ec-87d5-9d0651759595 36 fields · synced Jun 8, 2026