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Fenestrated Atraumatic Forceps Inner Shaft 43cm

FDA UDI

Class II (US FDA UDI)

by Orange Surgical Instruments, Llc

Identity

Trade Name
Fenestrated Atraumatic Forceps Inner Shaft 43cm FDA UDI
Generic Name
Endoscopic electrosurgical handpiece/electrode, monopolar, reusable FDA UDI
Device Name
Fenestrated Atraumatic Forceps Inner Shaft 43cm FDA UDI
Model / Reference
C279B FDA UDI
Description
Fenestrated Atraumatic Forceps Inner Shaft 43cm FDA UDI

Identifiers

Primary DI / UDI-DI
B354C279B2 FDA UDI
B354C279B9 FDA UDI
510(k) Number
K101733 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Endoscopic electrosurgical handpiece/electrode, monopolar, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 FDA UDI
Commercial Distribution
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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Peracetic Acid FDA UDI

Category: Endoscopic electrosurgical handpiece/electrode, monopolar, reusableEndoscopic electrosurgical electrode, monopolar, single-use

Fenestrated Atraumatic Forceps Inner Shaft 43cm by Orange Surgical Instruments, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic electrosurgical electrode, monopolar, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI 2ac407ac-a569-4836-b23d-d200d3d9804b 34 fields · synced Jun 8, 2026
  • FDA UDI dd72b1a9-8167-496a-8f8d-a09d25172a71 34 fields · synced May 27, 2026