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SCANLAN® Advantage™ Badie™ Suction Bipolar Forceps

FDA UDI

Class II (US FDA UDI)

by Scanlan International Inc

Identity

Trade Name
SCANLAN® Advantage™ Badie™ Suction Bipolar Forceps FDA UDI
Generic Name
Electrosurgical handpiece, reusable FDA UDI
Device Name
SCANLAN® Advantage™ Badie™ Bipolar Forceps FDA UDI
Model / Reference
4004-407 FDA UDI
Description
SCANLAN® Advantage™ Badie™ Bipolar Forceps FDA UDI

Identifiers

Catalog Number
4004-407 FDA UDI
Primary DI / UDI-DI
00846159016789 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Electrosurgical handpiece, 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Electrosurgical handpiece, reusable

SCANLAN® Advantage™ Badie™ Suction Bipolar Forceps by Scanlan International Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrosurgical handpiece, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Scanlan International Inc

Sources (1)

  • FDA UDI 7b3aca09-e4d2-4543-91ca-f5fea274cb62 35 fields · synced May 30, 2026