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Scleral Buckling Product Style 505T, 5.0mm Round Tunel Sponge

FDA UDI

Class II (US FDA UDI)

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

Identity

Trade Name
Scleral Buckling Product Style 505T, 5.0mm Round Tunel Sponge FDA UDI
Generic Name
Scleral buckling device, non-bioabsorbable FDA UDI
Model / Reference
92-50-32G FDA UDI

Identifiers

Catalog Number
92-50-32G FDA UDI
Primary DI / UDI-DI
08717872014555 FDA UDI
510(k) Number
K023481 FDA UDI
FDA Product Code
HQX FDA UDI
GMDN Term
Scleral buckling device, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.3340 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Scleral buckling device, non-bioabsorbable

Scleral Buckling Product Style 505T, 5.0mm Round Tunel Sponge by D.O.R.C. Dutch Ophthalmic Research Center (International) B.V. — Class II — FDA UDI — listed…

Similar devices

Also classified as Scleral buckling device, non-bioabsorbable.

Cleared under the same submission

K023481 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7021368b-70b3-4197-b4be-cfd5ad4f2063 34 fields · synced Jun 6, 2026