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Biliary Plastic Stent Set

FDA UDI

Class II (US FDA UDI)

by Micro-Tech (Nanjing) Co., Ltd.

Identity

Trade Name
Biliary Plastic Stent Set FDA UDI
Generic Name
Biliary drain FDA UDI
Device Name
TPU,Side bend,10Fr,15cm working length with 2200mm introducer FDA UDI
Model / Reference
BPDS-43114-1015/22 FDA UDI
Description
TPU,Side bend,10Fr,15cm working length with 2200mm introducer FDA UDI

Identifiers

Primary DI / UDI-DI
06932503514125 FDA UDI
510(k) Number
K230127 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Dimensions & Sizes

Size
Stent Diameter — 3.3 Millimeter FDA UDI
Stent Length — 150 Millimeter FDA UDI

Category: Biliary drain

Biliary Plastic Stent Set by Micro-Tech (Nanjing) Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Biliary drain.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 51503a65-6aab-4719-bc80-30062597abd0 36 fields · synced May 30, 2026