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Miller

FDA UDI

Class II (US FDA UDI)

by Cook Incorporated

Identity

Trade Name
Miller FDA UDI
Generic Name
Biliary drain FDA UDI
Device Name
Miller Double Mushroom Biliary Stent Set FDA UDI
Model / Reference
G03412 FDA UDI
Description
Miller Double Mushroom Biliary Stent Set FDA UDI

Identifiers

Catalog Number
UBSS-10-5.0-MLR FDA UDI
Primary DI / UDI-DI
00827002034129 FDA UDI
FDA Product Code
FGE FDA UDI
GMDN Term
Biliary drain FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5010 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

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Biliary drain

Miller by Cook Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Biliary drain.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cook Incorporated

Sources (1)

  • FDA UDI 118da9f6-30c4-42fc-9e63-f4e0235662b7 36 fields · synced Jun 6, 2026