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Breeze Centesis Drainage Catheter

FDA UDI

Class I (US FDA UDI)

by Medical Components Inc

Identity

Trade Name
BREEZE CENTESIS DRAINAGE CATHETER FDA UDI
Generic Name
Abdominal paracentesis needle, single-use FDA UDI
Device Name
5F X 10CM BREEZE STRAIGHT SLIP FIT CENTESIS DRAINAGE CATHETER FDA UDI
Model / Reference
CESSF5100 FDA UDI
Description
5F X 10CM BREEZE STRAIGHT SLIP FIT CENTESIS DRAINAGE CATHETER FDA UDI

Identifiers

Catalog Number
CESSF5100 FDA UDI
Primary DI / UDI-DI
00884908163780 FDA UDI
FDA Product Code
GBX FDA UDI
GMDN Term
Abdominal paracentesis needle, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4200 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: Abdominal paracentesis needle, single-use

Breeze Centesis Drainage Catheter by Medical Components Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Abdominal paracentesis needle, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 436e6713-277e-46b0-89e9-181626518f6c 35 fields · synced Jun 1, 2026