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Bard® Intra-abdominal Pressure Monitoring Device

FDA UDI

Class U (US FDA UDI)

by C. R. Bard, Inc.

Identity

Trade Name
Bard® Intra-abdominal Pressure Monitoring Device FDA UDI
Generic Name
Intra-abdominal pressure measurement set, mechanical FDA UDI
Device Name
Bard Intra-abdominal Pressure Monitoring Device FDA UDI
Model / Reference
IAP001 FDA UDI
Description
Bard Intra-abdominal Pressure Monitoring Device FDA UDI

Identifiers

Catalog Number
IAP001 FDA UDI
Primary DI / UDI-DI
00801741121098 FDA UDI
FDA Product Code
PHU FDA UDI
GMDN Term
Intra-abdominal pressure measurement set, mechanical FDA UDI

Classification

Device Class
U 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

Category: Intra-abdominal pressure measurement set, mechanical

Bard® Intra-abdominal Pressure Monitoring Device by C. R. Bard, Inc. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intra-abdominal pressure measurement set, mechanical.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
C. R. Bard, Inc.

Sources (1)

  • FDA UDI 56691321-6694-434a-ac9b-38be9d8ddb30 35 fields · synced May 30, 2026