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Desilets-Hoffman

FDA UDI

Class II (US FDA UDI)

by Cook Incorporated

Identity

Trade Name
Desilets-Hoffman FDA UDI
Generic Name
Ureteral introduction sheath FDA UDI
Device Name
Desilets-Hoffman Introducer Set With Radiopaque Band FDA UDI
Model / Reference
G18089 FDA UDI
Description
Desilets-Hoffman Introducer Set With Radiopaque Band FDA UDI

Identifiers

Catalog Number
DHIS-080030-RB-DIL88 FDA UDI
Primary DI / UDI-DI
00827002180895 FDA UDI
FDA Product Code
EZN FDA UDI
GMDN Term
Ureteral introduction sheath FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5470 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

Yes

FDA UDI

Category: Ureteral introduction sheath

Desilets-Hoffman by Cook Incorporated — 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
Cook Incorporated

Sources (1)

  • FDA UDI 28bc7a7b-62e2-436e-a283-5db2b1b4253f 36 fields · synced Jun 8, 2026