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Soehendra

FDA UDI

Class II (US FDA UDI)

by Cook Incorporated

Identity

Trade Name
Soehendra FDA UDI
Generic Name
Flexible endoscopic tissue manipulation forceps, single-use FDA UDI
Device Name
Soehendra Stent Retriever FDA UDI
Model / Reference
G21535 FDA UDI
Description
Soehendra Stent Retriever FDA UDI

Identifiers

Catalog Number
SSR-11.5 FDA UDI
Primary DI / UDI-DI
00827002215351 FDA UDI
FDA Product Code
FGE FDA UDI
GMDN Term
Flexible endoscopic tissue manipulation forceps, single-use 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

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: Flexible endoscopic tissue manipulation forceps, single-use

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

Similar devices

Also classified as Flexible endoscopic tissue manipulation forceps, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cook Incorporated

Sources (1)

  • FDA UDI c9f6fbeb-23ba-4b09-8d24-e10007fd3252 36 fields · synced Jun 8, 2026