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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
Instrument transport trolley system FDA UDI
Device Name
SCHWERT Protector-Tray, 1/2 for 8 instruments with 2 instrument support and 1 retainer, 178 x 140 x 24 mm FDA UDI
Model / Reference
2597-08 FDA UDI
Description
SCHWERT Protector-Tray, 1/2 for 8 instruments with 2 instrument support and 1 retainer, 178 x 140 x 24 mm FDA UDI

Identifiers

Catalog Number
2597-08 FDA UDI
Primary DI / UDI-DI
E8962597080 FDA UDI
FDA Product Code
FSM FDA UDI
GMDN Term
Instrument transport trolley system 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Instrument transport trolley system

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

Similar devices

Also classified as Instrument transport trolley system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 59970a13-aa0b-44e0-a0ab-84d9d19e3c20 35 fields · synced May 31, 2026