← Back to catalogue

Hayden Medical

FDA UDI

Class I (US FDA UDI)

by Hayden Medical Inc

Identity

Trade Name
Hayden Medical FDA UDI
Generic Name
Common bile duct dilator FDA UDI
Device Name
Bakes Common Duct Dilator Set,8-1/4"(21.0cm), in canvas roll cotaining 9 dilators sizes 3mm to 11mm, malleable shafts FDA UDI
Model / Reference
290-419 FDA UDI
Description
Bakes Common Duct Dilator Set,8-1/4"(21.0cm), in canvas roll cotaining 9 dilators sizes 3mm to 11mm, malleable shafts FDA UDI

Identifiers

Catalog Number
290-419 FDA UDI
Primary DI / UDI-DI
00840319748282 FDA UDI
FDA Product Code
FGM FDA UDI
GMDN Term
Common bile duct dilator FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.4730 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Common bile duct dilator

Hayden Medical by Hayden Medical Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Common bile duct dilator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Hayden Medical Inc

Sources (1)

  • FDA UDI a2f608bf-b1f0-4d98-a9c4-53a184b0e14c 35 fields · synced Jun 8, 2026