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Atlanta Healthcare Services OcuDrape®

FDA UDI

Class II (US FDA UDI)

by Atlanta Healthcare Services

Identity

Trade Name
Atlanta Healthcare Services OcuDrape® FDA UDI
Generic Name
Ophthalmic sponge FDA UDI
Device Name
PVA Instrument Wipe Kit, 2IN1 Wipe & Eye Drain Wick,Corneal Light Shield Non-sterile FDA UDI
Model / Reference
10852171007763 FDA UDI
Description
PVA Instrument Wipe Kit, 2IN1 Wipe & Eye Drain Wick,Corneal Light Shield Non-sterile FDA UDI

Identifiers

Catalog Number
S320NS FDA UDI
Primary DI / UDI-DI
10852171007763 FDA UDI
510(k) Number
K942642 FDA UDI
FDA Product Code
HOZ FDA UDI
GMDN Term
Ophthalmic sponge FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.4790 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Width — 3.15 Inch FDA UDI
Length — 3 Inch FDA UDI

Category: Ophthalmic sponge

Atlanta Healthcare Services OcuDrape® by Atlanta Healthcare Services — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic sponge.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8609baa2-dd0d-4b2d-9bf1-e1fbc67cee5b 37 fields · synced May 30, 2026