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Accessories, arthroscopic

FDA UDI

Class I (US FDA UDI)

by Parcus Medical Llc

Identity

Trade Name
Accessories, arthroscopic FDA UDI
Generic Name
Surgical instrument/implant rack FDA UDI
Device Name
Mat, Universal Instrument Tray FDA UDI
Model / Reference
20190 FDA UDI
Description
Mat, Universal Instrument Tray FDA UDI

Identifiers

Primary DI / UDI-DI
00816342025096 FDA UDI
FDA Product Code
NBH FDA UDI
GMDN Term
Surgical instrument/implant rack FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.1100 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical instrument/implant rack

Accessories, arthroscopic by Parcus Medical Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical instrument/implant rack.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Parcus Medical Llc

Sources (1)

  • FDA UDI 7c762a84-37ae-4da8-baf4-751b9cf7a81c 33 fields · synced May 30, 2026