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Plate Holding Forceps

FDA UDI

Class II (US FDA UDI)

by I.T.S. GmbH

Identity

Trade Name
Plate Holding Forceps FDA UDI
Generic Name
Flexible endoscopic scissors, reusable FDA UDI
Device Name
Plate Holding Forceps, 15.5cm FDA UDI
Model / Reference
06-586 FDA UDI
Description
Plate Holding Forceps, 15.5cm FDA UDI

Identifiers

Catalog Number
06-586 FDA UDI
Primary DI / UDI-DI
09120047306062 FDA UDI
FDA Product Code
KTT FDA UDI
GMDN Term
Flexible endoscopic scissors, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Flexible endoscopic scissors, reusable

Plate Holding Forceps by I.T.S. GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Flexible endoscopic scissors, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
I.T.S. GmbH

Sources (1)

  • FDA UDI 34e64fda-ae9f-4d73-8fc7-5fa1a8403736 34 fields · synced Jun 8, 2026