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Eg1™

FDA UDI

Class II (US FDA UDI)

by Anspach Effort, The

Identity

Trade Name
EG1™ FDA UDI
Generic Name
Surgical power tool hand-switch FDA UDI
Device Name
Wireless Hand Control, EG1A FDA UDI
Model / Reference
WIRELESS-HC FDA UDI
Description
Wireless Hand Control, EG1A FDA UDI

Identifiers

Catalog Number
WIRELESS-HC FDA UDI
Primary DI / UDI-DI
00845384018759 FDA UDI
510(k) Number
K220485 FDA UDI
FDA Product Code
ERL FDA UDI
HBC FDA UDI
GMDN Term
Surgical power tool hand-switch FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.4250 FDA UDI
882.4360 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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Surgical power tool hand-switch

Eg1™ by Anspach Effort, The — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical power tool hand-switch.

Cleared under the same submission

K220485 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Anspach Effort, The

Sources (1)

  • FDA UDI 1c094402-f5f4-45f3-a834-78cb43af2869 37 fields · synced May 30, 2026