Surgyco PS010115

Surgyco PS010115 is a Class I device made by Surgyco LLC, listed in FDA GUDID since 16 Feb 2023 (UDI-DI 10850044799722), 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	Number10850044799722 UDI-DI	Date16 Feb 2023Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 10850044799722

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Withdrawn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: PS010115

Primary DI / UDI-DI: 10850044799722
FDA product code: OEA
GMDN term: General-purpose syringe, single-use

Device class: Class I
Regulation number: 878.4040
GUDID distribution status: In Commercial Distribution

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Properties

Single use
Contains latex
Premarket exempt
Lot / batch number
Manufacturing date

Other properties (10, all answered No)