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27G High Flow infusion line

FDA UDI

Class I (US FDA UDI)

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

Identity

Trade Name
27G High Flow infusion line FDA UDI
Generic Name
Ophthalmic cannulation set, single-use FDA UDI
Model / Reference
1279.HF27 FDA UDI

Identifiers

Catalog Number
1279.HF27 FDA UDI
Primary DI / UDI-DI
08717872032412 FDA UDI
FDA Product Code
NGY FDA UDI
GMDN Term
Ophthalmic cannulation set, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4350 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Ophthalmic cannulation set, single-use

27G High Flow infusion line by D.O.R.C. Dutch Ophthalmic Research Center (International) B.V. — Class I — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Ophthalmic cannulation set, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9a63156b-5aa9-43b6-9e97-7265c4dd9ebb 33 fields · synced Jun 1, 2026