Walcott Rx Products Rx282

by Walcott Rx Product Inc

Walcott Rx Products Rx282 is a Class I device made by Walcott Rx Product Inc, listed in FDA GUDID since 10 Aug 2022 (UDI-DI 00840285318410), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00840285318410 UDI-DI	Date10 Aug 2022Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00840285318410

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Walcott Rx Products
Generic name: Ophthalmic surgical device handling forceps, reusable
Model / reference: Rx282

Primary DI / UDI-DI: 00840285318410
FDA product code: HNR
GMDN term: Ophthalmic surgical device handling forceps, reusable

Device class: Class I
Regulation number: 886.4350
GUDID distribution status: In Commercial Distribution

Sterilisation method: Moist Heat or Steam Sterilization

Similar devices in this category

Other devices filed under Ophthalmic surgical device handling forceps, reusable.

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Class I

See all devices from Walcott Rx Product Inc →

Properties

Sterilise before use
Premarket exempt
Lot / batch number

Other properties (12, all answered No)