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Active Cord Reusable Bovie

FDA UDI

Class II (US FDA UDI)

by Micro-tech Usa

Identity

Trade Name
Active Cord Reusable Bovie FDA UDI
Generic Name
Electrical-only medical device connection cable, reusable FDA UDI
Device Name
Active Cord Reusable Bovie FDA UDI
Model / Reference
AEC-03-08 FDA UDI
Description
Active Cord Reusable Bovie FDA UDI

Identifiers

Primary DI / UDI-DI
00850025860253 FDA UDI
510(k) Number
K974793 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Electrical-only medical device connection cable, 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Electrical-only medical device connection cable, reusable

Active Cord Reusable Bovie by Micro-tech Usa — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrical-only medical device connection cable, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Micro-tech Usa

Sources (1)

  • FDA UDI 74c93650-cc4a-430d-9fd9-e695c499747a 34 fields · synced May 31, 2026