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Manual Infusion Pole. Accessory to the DORC Trolley

FDA UDI

Class II (US FDA UDI)

by D.O.R.C. Dutch Ophthalmic Research Center (International) B.V.

Identity

Trade Name
Manual Infusion Pole. Accessory to the DORC Trolley FDA UDI
Generic Name
Electromechanical device/system transport trolley FDA UDI
Model / Reference
6005.A1 FDA UDI

Identifiers

Catalog Number
6005.A1 FDA UDI
Primary DI / UDI-DI
08717872019437 FDA UDI
510(k) Number
K081877 FDA UDI
FDA Product Code
HQC FDA UDI
GMDN Term
Electromechanical device/system transport trolley FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.4670 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Electromechanical device/system transport trolley

Manual Infusion Pole. Accessory to the DORC Trolley by D.O.R.C. Dutch Ophthalmic Research Center (International) B.V. — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Electromechanical device/system transport trolley.

Cleared under the same submission

K081877 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2164d71a-7bbb-4d45-a6a6-eb7e1ea05e68 34 fields · synced Jun 8, 2026