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21000 ES Pencil Holster

FDA UDI

Class II (US FDA UDI)

by Xodus Medical, Inc.

Identity

Trade Name
21000 ES Pencil Holster FDA UDI
Generic Name
Electrosurgical handpiece, single-use FDA UDI
Device Name
21000 ES Pencil Holster FDA UDI
Model / Reference
21000 FDA UDI
Description
21000 ES Pencil Holster FDA UDI

Identifiers

Catalog Number
21000 FDA UDI
Primary DI / UDI-DI
00787551035117 FDA UDI
510(k) Number
K081647 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Electrosurgical handpiece, single-use 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

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Radiation Sterilization FDA UDI

Category: Electrosurgical handpiece, single-use

21000 ES Pencil Holster by Xodus Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrosurgical handpiece, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Xodus Medical, Inc.

Sources (1)

  • FDA UDI 845370ae-1653-457a-ba45-262abec633a7 36 fields · synced May 30, 2026