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Curved Down Forceps, Bayonet Handle, .3mm Tips, 210mm

FDA UDI

Class I (US FDA UDI)

by Katalyst Surgical, Llc

Identity

Trade Name
Curved Down Forceps, Bayonet Handle, .3mm Tips, 210mm FDA UDI
Generic Name
Dissection forceps FDA UDI
Device Name
Each, Dissection Forceps, 210mm FDA UDI
Model / Reference
N3207 FDA UDI
Description
Each, Dissection Forceps, 210mm FDA UDI

Identifiers

Primary DI / UDI-DI
00856312006373 FDA UDI
FDA Product Code
HTD FDA UDI
GMDN Term
Dissection forceps FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

No

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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dissection forceps

Curved Down Forceps, Bayonet Handle, .3mm Tips, 210mm by Katalyst Surgical, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dissection forceps.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Katalyst Surgical, Llc

Sources (1)

  • FDA UDI c18c736f-9d58-49e6-9125-8ce75fb22137 33 fields · synced May 30, 2026