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BioCeps Biopsy Forceps

FDA UDI

Class II (US FDA UDI)

by Endo-Therapeutics, Inc.

Identity

Trade Name
BioCeps Biopsy Forceps FDA UDI
Generic Name
Endoscopic electrosurgical handpiece/electrode, monopolar, single-use FDA UDI
Device Name
Endoscopic Biopsy Forceps - Hot FDA UDI
Model / Reference
ET1402 FDA UDI
Description
Endoscopic Biopsy Forceps - Hot FDA UDI

Identifiers

Catalog Number
ET1402 FDA UDI
Primary DI / UDI-DI
00816207021423 FDA UDI
510(k) Number
K800973 FDA UDI
FDA Product Code
KNS FDA UDI
GMDN Term
Endoscopic electrosurgical handpiece/electrode, monopolar, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.4300 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

Dimensions & Sizes

Size
Length — 160 Centimeter FDA UDI
Outer Diameter — 2.4 Millimeter FDA UDI

Category: Endoscopic electrosurgical handpiece/electrode, monopolar, single-use

BioCeps Biopsy Forceps by Endo-Therapeutics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic electrosurgical handpiece/electrode, monopolar, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d10c34f1-fc55-41ac-b328-ff5cdbc483ca 38 fields · synced May 31, 2026