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IN CUT scissors

FDA UDI

Class II (US FDA UDI)

by Peters Surgical

Identity

Trade Name
IN CUT scissors FDA UDI
Generic Name
Endoscopic electrosurgical electrode, monopolar, single-use FDA UDI
Device Name
Single use, monopolar cautery scissors (curved blade) for laparoscopic surgery FDA UDI
Model / Reference
T5330 FDA UDI
Description
Single use, monopolar cautery scissors (curved blade) for laparoscopic surgery FDA UDI

Identifiers

Catalog Number
T5330 FDA UDI
Primary DI / UDI-DI
03700393300066 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Endoscopic electrosurgical electrode, monopolar, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 FDA UDI
Commercial Distribution
Not 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
Outer Diameter — 5 Millimeter FDA UDI
Length — 330 Millimeter FDA UDI

IN CUT scissors by Peters Surgical — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Peters Surgical

Sources (1)

  • FDA UDI e9827d38-a38c-48dc-bb20-38a84c1e9f90 37 fields · synced May 31, 2026