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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
Syndesmotome FDA UDI
Device Name
Knife, periodontic, KGF8, modif. Double ended, SWORD DESIGN handle 17,5cm, 2,4mm FDA UDI
Model / Reference
1705-65 FDA UDI
Description
Knife, periodontic, KGF8, modif. Double ended, SWORD DESIGN handle 17,5cm, 2,4mm FDA UDI

Identifiers

Catalog Number
1705-65 FDA UDI
Primary DI / UDI-DI
E8961705650 FDA UDI
FDA Product Code
EMK FDA UDI
GMDN Term
Syndesmotome 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

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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Syndesmotome

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

Similar devices

Also classified as Syndesmotome.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
A. Schweickhardt GmbH & Co. KG

Sources (1)

  • FDA UDI e077a9b6-e85f-44c0-97b4-b259bb597b4d 35 fields · synced May 30, 2026