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PeritX

FDA UDI

Class II (US FDA UDI)

by Carefusion 2200, Inc

Identity

Trade Name
PeritX FDA UDI
Generic Name
Closed-wound/centesis drainage receptacle FDA UDI
Device Name
PeritX Drainage Kit, 2000 mL FDA UDI
Model / Reference
50-9510 FDA UDI
Description
PeritX Drainage Kit, 2000 mL FDA UDI

Identifiers

Catalog Number
50-9510 FDA UDI
Primary DI / UDI-DI
10885403222412 FDA UDI
FDA Product Code
PNG FDA UDI
GMDN Term
Closed-wound/centesis drainage receptacle FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5630 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Total Volume — 2000 Milliliter FDA UDI

Category: Closed-wound/centesis drainage receptacle

PeritX by Carefusion 2200, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Closed-wound/centesis drainage receptacle.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 06e0da1a-0a9a-40a8-a0af-99a69a864f97 36 fields · synced Jun 8, 2026