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Key Surgical Foreign Body Retrievers

FDA UDI

Class I (US FDA UDI)

by Key Surgical, LLC

Identity

Trade Name
Key Surgical Foreign Body Retrievers FDA UDI
Generic Name
Flexible endoscopic tissue manipulation forceps, single-use FDA UDI
Device Name
Retrieval Net, 2.3mm Diam, 1800mm L, 30mm (Net) W, 60mm (Net) H FDA UDI
Model / Reference
EN10179B FDA UDI
Description
Retrieval Net, 2.3mm Diam, 1800mm L, 30mm (Net) W, 60mm (Net) H FDA UDI

Identifiers

Primary DI / UDI-DI
00849771039914 FDA UDI
FDA Product Code
GDJ FDA UDI
GMDN Term
Flexible endoscopic tissue manipulation forceps, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
Not 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

No

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

Dimensions & Sizes

Size
Outer Diameter — 2.3 Millimeter FDA UDI
Length — 1800 Millimeter FDA UDI
Width — 30 Millimeter FDA UDI
Height — 60 Millimeter FDA UDI

Key Surgical Foreign Body Retrievers by Key Surgical, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Key Surgical, LLC

Sources (1)

  • FDA UDI 21071cd3-9aa3-412c-8e06-b69111321d14 36 fields · synced Jun 1, 2026