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Surgyco

FDA UDI

Class I (US FDA UDI)

by Surgyco LLC

Identity

Trade Name
SURGYCO FDA UDI
Generic Name
General-purpose syringe, single-use FDA UDI
Device Name
Lap Sponge, Sterile, X-Ray Detectable, Pre-Washed 18" x 18" FDA UDI
Model / Reference
GS000435 FDA UDI
Description
Lap Sponge, Sterile, X-Ray Detectable, Pre-Washed 18" x 18" FDA UDI

Identifiers

Primary DI / UDI-DI
10850049784433 FDA UDI
FDA Product Code
GDY FDA UDI
GMDN Term
General-purpose syringe, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4450 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: General-purpose syringe, single-use

Surgyco by Surgyco LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose syringe, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Surgyco LLC

Sources (1)

  • FDA UDI 46f5f38a-f831-452d-9268-43fa58d37d4e 33 fields · synced May 30, 2026