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Wexler Surgical, Inc.

FDA UDI

Class I (US FDA UDI)

by Wexler Surgical, Inc.

Identity

Trade Name
Wexler Surgical, Inc. FDA UDI
Generic Name
Corneal bur, rust ring removal, reusable FDA UDI
Model / Reference
BL0010.4-1 FDA UDI

Identifiers

Primary DI / UDI-DI
M944BL0010410 FDA UDI
FDA Product Code
OHW FDA UDI
GMDN Term
Corneal bur, rust ring removal, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4070 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

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: Corneal bur, rust ring removal, reusable

Wexler Surgical, Inc. by Wexler Surgical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Corneal bur, rust ring removal, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Wexler Surgical, Inc.

Sources (1)

  • FDA UDI bb544a98-ce53-4858-9f43-5bed2293d0bf 32 fields · synced Jun 9, 2026