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Aspira Drainage Supplies

FDA UDI

Class II (US FDA UDI)

by Bard Access Systems, Inc.

Identity

Trade Name
Aspira Drainage Supplies FDA UDI
Generic Name
Pleural/peritoneal drainage catheterization kit FDA UDI
Device Name
Aspira Peritoneal Complete Drainage Supplies FDA UDI
Model / Reference
4992207B FDA UDI
Description
Aspira Peritoneal Complete Drainage Supplies FDA UDI

Identifiers

Catalog Number
4992207B FDA UDI
Primary DI / UDI-DI
10801741091183 FDA UDI
FDA Product Code
FJS 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 — 1 Liter FDA UDI

Category: Pleural/peritoneal drainage catheterization kit

Aspira Drainage Supplies by Bard Access Systems, Inc. — 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 Access Systems, Inc.

Sources (1)

  • FDA UDI ed35c243-7618-4b2f-a1b0-abb92de631d2 36 fields · synced Jun 9, 2026