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Replacement clear plastic attachments for Durette® III (nasals only) (10 units)

FDA UDI

Class I (US FDA UDI)

by Oculo-Plastik Inc

Identity

Trade Name
Replacement clear plastic attachments for Durette® III (nasals only) (10 units) FDA UDI
Generic Name
Epiocular radiation shield, reusable FDA UDI
Device Name
Replacement clear plastic attachments for Durette III (nasals only) (10 units) FDA UDI
Model / Reference
21-440N FDA UDI
Description
Replacement clear plastic attachments for Durette III (nasals only) (10 units) FDA UDI

Identifiers

Primary DI / UDI-DI
20697660002419 FDA UDI
FDA Product Code
IWS FDA UDI
GMDN Term
Epiocular radiation shield, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
892.6500 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

Yes

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
Liquid Chemical FDA UDI

Category: Epiocular radiation shield, reusable

Replacement clear plastic attachments for Durette® III (nasals only) (10 units) by Oculo-Plastik Inc — Class I — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Epiocular radiation shield, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Oculo-Plastik Inc

Sources (1)

  • FDA UDI c7c06c02-20b5-455e-ab49-81fc1a94d73d 34 fields · synced May 30, 2026