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Schwert

FDA UDI

Class I (US FDA UDI)

by A. Schweickhardt GmbH & Co. KG

Identity

Trade Name
SCHWERT FDA UDI
Generic Name
Surgical flat-nosed pliers FDA UDI
Device Name
Wire seizing forceps, TC, 16cm, 5 1/2" FDA UDI
Model / Reference
14165-16 FDA UDI
Description
Wire seizing forceps, TC, 16cm, 5 1/2" FDA UDI

Identifiers

Catalog Number
14165-16 FDA UDI
Primary DI / UDI-DI
E89614165160 FDA UDI
FDA Product Code
EMH FDA UDI
GMDN Term
Surgical flat-nosed pliers FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical flat-nosed pliers

Schwert by A. Schweickhardt GmbH & Co. KG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical flat-nosed pliers.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 96e2f17c-272a-4c08-a8c5-7a890246d9b8 35 fields · synced May 30, 2026