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PeritX

FDA UDI

Class II (US FDA UDI)

by Bard Peripheral Vascular

Identity

Trade Name
PeritX FDA UDI
Generic Name
Pleural/peritoneal drainage catheterization kit FDA UDI
Device Name
PeritX™ 2L Drainage Starter Pack FDA UDI
Model / Reference
90-2020 FDA UDI
Description
PeritX™ 2L Drainage Starter Pack FDA UDI

Identifiers

Catalog Number
90-2020 FDA UDI
Primary DI / UDI-DI
00801741230639 FDA UDI
FDA Product Code
PNG FDA UDI
GMDN Term
Pleural/peritoneal drainage catheterization kit 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

Yes

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 — 2 Liter FDA UDI

Category: Pleural/peritoneal drainage catheterization kit

PeritX by Bard Peripheral Vascular — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pleural/peritoneal drainage catheterization kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bard Peripheral Vascular

Sources (1)

  • FDA UDI 0081bc0b-e6ba-4da1-8d01-28ea5360a6ed 36 fields · synced Jun 8, 2026