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Ambler Surgical

FDA UDI

Class I (US FDA UDI)

by Ambler Surgical, LLC

Identity

Trade Name
Ambler Surgical FDA UDI
Generic Name
Ophthalmic surgery fluid retention ring FDA UDI
Device Name
Hyver PRK/LASEK alcohol well, 3 3/4'', 7.5mm x 8.5mm oval diameter, 3.0mm ring height, semi-sharp bottom edge, used to limit the extent of epithelium removal for mixed astigmatism treatment, round handle FDA UDI
Model / Reference
Hyver PRK/LASEK alcohol well FDA UDI
Description
Hyver PRK/LASEK alcohol well, 3 3/4'', 7.5mm x 8.5mm oval diameter, 3.0mm ring height, semi-sharp bottom edge, used to limit the extent of epithelium removal for mixed astigmatism treatment, round handle FDA UDI

Identifiers

Catalog Number
8898E FDA UDI
Primary DI / UDI-DI
00190660000301 FDA UDI
FDA Product Code
HNH FDA UDI
GMDN Term
Ophthalmic surgery fluid retention ring 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

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

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
Moist Heat or Steam Sterilization FDA UDI

Category: Ophthalmic surgery fluid retention ring

Ambler Surgical by Ambler Surgical, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic surgery fluid retention ring.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5cab09ff-e5e3-450e-bcd8-913a8d3ee3a0 35 fields · synced May 30, 2026