Surgyco RS000390

Surgyco RS000390 is a Class I device made by Surgyco LLC, listed in FDA GUDID since 31 Oct 2023 (UDI-DI 10850049784808), 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	Number10850049784808 UDI-DI	Date31 Oct 2023Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 10850049784808

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Surgyco
Generic name: General-purpose syringe, single-use
Model / reference: RS000390

Primary DI / UDI-DI: 10850049784808
FDA product code: BSY
GMDN term: General-purpose syringe, single-use

Device class: Class I
Regulation number: 868.6810
GUDID distribution status: In Commercial Distribution

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Properties

Supplied sterile
Single use
Premarket exempt
Lot / batch number
Expiration date
Manufacturing date

Other properties (9, all answered No)