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Boston XO2

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref Spec0347

by Bausch & Lomb Incorporated

Identity

Trade Name
Boston XO2 EUDAMEDFDA UDI
Generic Name
Rigid-gas-permeable corrective contact lens, daily-wear FDA UDI
Device Name
Boston XO2 (hexafocon B) Rigid Gas Permeable Contact Lenses EUDAMED
Rigid Gas Permeable Contact Lens FDA UDI
Model / Reference
Spec0347 EUDAMED
hexafocon B FDA UDI
Description
Rigid Gas Permeable Contact Lens FDA UDI

Identifiers

Catalog Number
Boston XO2 FDA UDI
Primary DI / UDI-DI
0196527M0070GX EUDAMED
00785811435677 FDA UDI
Basic UDI-DI
0310119B0031Z2 EUDAMED
FDA Product Code
HQD FDA UDI
EMDN Code
Q02100402 CONTACT LENSES - NON HYDROGEL EUDAMED
GMDN Term
Rigid-gas-permeable corrective contact lens, daily-wear FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
886.5916 FDA UDI
Special Device Type
Standard Rigid Gas Permeable (RGP) Contact Lenses EUDAMED
Market of Registration
Ireland EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Category: Rigid-gas-permeable corrective contact lens, daily-wear

Boston XO2 by Bausch & Lomb Incorporated — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Rigid-gas-permeable corrective contact lens, daily-wear.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI 30d72a08-8419-4a4c-8f59-092be5042b81 34 fields · synced Oct 6, 2026
  • EUDAMED 96d56b77-457b-4c97-bb27-a01d34996817 61 fields · synced Sep 17, 2026