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Long Fenestrated, - outer shaft

FDA UDI

Class II (US FDA UDI)

by Orange Surgical Instruments, Llc

Identity

Trade Name
Long Fenestrated, (1 Set: handle, inner shaft, outer shaft) FDA UDI
Generic Name
Endoscopic electrosurgical electrode, monopolar, single-use FDA UDI
Device Name
Long Fenestrated, (1 Set: handle, inner shaft, outer shaft) FDA UDI
Model / Reference
OS5339 FDA UDI
Description
Long Fenestrated, (1 Set: handle, inner shaft, outer shaft) FDA UDI

Identifiers

Primary DI / UDI-DI
B354OS53390 FDA UDI
510(k) Number
K101733 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Endoscopic electrosurgical electrode, monopolar, single-use FDA UDI
Models / Variants
inner shaft FDA UDI
outer shaft FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI
Sterilization Method
Peracetic Acid FDA UDI

Long Fenestrated, - outer shaft by Orange Surgical Instruments, Llc — Class II — FDA UDI — listed in FDA GUDID — 3 models — regulatory data on deviCERTS

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 32de03de-a66a-43c3-b736-d64abe8afa5f 35 fields · synced Jun 8, 2026