Surgyco PSS10130

Surgyco PSS10130 is a Class I device made by Surgyco LLC, listed in FDA GUDID since 30 Jun 2023 (UDI-DI 10850044799876), 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	Number10850044799876 UDI-DI	Date30 Jun 2023Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 10850044799876

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Withdrawn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: PSS10130

Primary DI / UDI-DI: 10850044799876
FDA product code: KME
GMDN term: General-purpose syringe, single-use

Device class: Class I
Regulation number: 880.6060
GUDID distribution status: In Commercial Distribution

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Other devices filed under General-purpose syringe, single-use.

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Properties

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

Other properties (8, all answered No)