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Walcott Rx Products

FDA UDI

Class I (US FDA UDI)

by Walcott Rx Product Inc

Identity

Trade Name
Walcott Rx Products FDA UDI
Generic Name
Ophthalmic surgical device handling forceps, reusable FDA UDI
Device Name
Tying Forcep FDA UDI
Model / Reference
Rx282 FDA UDI
Description
Tying Forcep FDA UDI

Identifiers

Primary DI / UDI-DI
00840285318410 FDA UDI
FDA Product Code
HNR FDA UDI
GMDN Term
Ophthalmic surgical device handling forceps, reusable 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

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: Ophthalmic surgical device handling forceps, reusable

Walcott Rx Products by Walcott Rx Product Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic surgical device handling forceps, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Walcott Rx Product Inc

Sources (1)

  • FDA UDI dddee4de-6f5e-4437-81da-47a78f820a25 34 fields · synced May 30, 2026