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DinamicOR

FDA UDI

Class II (US FDA UDI)

by Paneffort, LLC

Identity

Trade Name
DinamicOR FDA UDI
Generic Name
Medical equipment/instrument drape, single-use FDA UDI
Device Name
DinamicOR Procedure Fee with Double-Wide Sterile Table Cover 12/case FDA UDI
Model / Reference
111-2112d FDA UDI
Description
DinamicOR Procedure Fee with Double-Wide Sterile Table Cover 12/case FDA UDI

Identifiers

Primary DI / UDI-DI
00810101311147 FDA UDI
FDA Product Code
PUI FDA UDI
GMDN Term
Medical equipment/instrument drape, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4370 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Medical equipment/instrument drape, single-use

DinamicOR by Paneffort, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical equipment/instrument drape, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Paneffort, LLC

Sources (1)

  • FDA UDI d1471da4-ca96-4514-909c-14866a06d780 35 fields · synced May 30, 2026