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AquaGuide® Ureteral Access Sheath

FDA UDI

Class II (US FDA UDI)

by C. R. Bard, Inc.

Identity

Trade Name
AquaGuide® Ureteral Access Sheath FDA UDI
Generic Name
Ureteral introduction sheath FDA UDI
Device Name
AquaGuide® Ureteral Access Sheath FDA UDI
Model / Reference
131235 FDA UDI
Description
AquaGuide® Ureteral Access Sheath FDA UDI

Identifiers

Catalog Number
131235 FDA UDI
Primary DI / UDI-DI
00801741052606 FDA UDI
FDA Product Code
FED FDA UDI
GMDN Term
Ureteral introduction sheath FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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

No

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
Length — 35 Centimeter FDA UDI

Category: Ureteral introduction sheath

AquaGuide® Ureteral Access Sheath by C. R. Bard, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ureteral introduction sheath.

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 b1dd9a3f-8545-494f-8612-079670d81151 36 fields · synced May 30, 2026