← Back to catalogue

Tungsten Needle Extended Ins +4 more models

FDA UDI

Class II (US FDA UDI)

by Xodus Medical, Inc.

Identity

Trade Name
Tungsten Needle Extended Ins; 45 degree; Blue Ins; Black Ext Ins; PL FDA UDI
Generic Name
Open-surgery electrosurgical electrode, monopolar, single-use FDA UDI
Model / Reference
20103ACT FDA UDI

Identifiers

Primary DI / UDI-DI
00787551002393 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Open-surgery electrosurgical electrode, monopolar, single-use FDA UDI
Models / Variants
Tungsten Needle Extended Ins FDA UDI
45 degree FDA UDI
Blue Ins FDA UDI
Black Ext Ins FDA UDI
PL 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

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Open-surgery electrosurgical electrode, monopolar, single-use

Tungsten Needle Extended Ins +4 more models by Xodus Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — 5 models — regulatory data on deviCERTS

Similar devices

Also classified as Open-surgery electrosurgical electrode, monopolar, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Xodus Medical, Inc.

Sources (1)

  • FDA UDI 137a75b3-0f48-4145-8a44-77c718a0f2ce 33 fields · synced May 31, 2026