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Hensler Surgical Disposable Non-Stick Bipolar

FDA UDI

Class II (US FDA UDI)

by Hensler Surgical

Identity

Trade Name
Hensler Surgical Disposable Non-Stick Bipolar FDA UDI
Generic Name
Open-surgery electrosurgical handpiece/electrode, bipolar, single-use FDA UDI
Device Name
Bayoneted bipolar forcep, Non-stick, single-use, yellow, 9" length, 1.5 mm tip, STERILE FDA UDI
Model / Reference
HSP-008 FDA UDI
Description
Bayoneted bipolar forcep, Non-stick, single-use, yellow, 9" length, 1.5 mm tip, STERILE FDA UDI

Identifiers

Primary DI / UDI-DI
00853755004270 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Open-surgery electrosurgical handpiece/electrode, bipolar, 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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 9 Inch FDA UDI

Category: Open-surgery electrosurgical handpiece/electrode, bipolar, single-use

Hensler Surgical Disposable Non-Stick Bipolar by Hensler Surgical — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Open-surgery electrosurgical handpiece/electrode, bipolar, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hensler Surgical

Sources (1)

  • FDA UDI 310c802d-0f35-49dd-b383-f62207522636 35 fields · synced May 30, 2026