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Johlin

FDA UDI

Class II (US FDA UDI)

by Cook Ireland, Ltd.

Identity

Trade Name
Johlin FDA UDI
Generic Name
Polymeric pancreatic stent, non-bioabsorbable FDA UDI
Device Name
Johlin, Pancreatic Wedge Stent FDA UDI
Model / Reference
G25713 FDA UDI
Description
Johlin, Pancreatic Wedge Stent FDA UDI

Identifiers

Catalog Number
JPWS-10-8 FDA UDI
Primary DI / UDI-DI
10827002257136 FDA UDI
FDA Product Code
FGE FDA UDI
GMDN Term
Polymeric pancreatic stent, non-bioabsorbable 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

Yes

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Polymeric pancreatic stent, non-bioabsorbable

Johlin by Cook Ireland, Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polymeric pancreatic stent, non-bioabsorbable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cook Ireland, Ltd.

Sources (1)

  • FDA UDI 7661f33f-a3ee-4874-97f8-b456a4ce6fd5 36 fields · synced Jun 8, 2026