← Back to catalogue

Surgyco

FDA UDI

Class II (US FDA UDI)

by Surgyco LLC

Identity

Trade Name
SURGYCO FDA UDI
Generic Name
General-purpose syringe, single-use FDA UDI
Device Name
VAGINAL SPECULUM SMALL DISPOSABLE. FDA UDI
Model / Reference
STV00100 FDA UDI
Description
VAGINAL SPECULUM SMALL DISPOSABLE. FDA UDI

Identifiers

Primary DI / UDI-DI
10850053289269 FDA UDI
FDA Product Code
HIB FDA UDI
GMDN Term
General-purpose syringe, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.4530 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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 II — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Surgyco LLC

Sources (1)

  • FDA UDI 9131fc4e-4986-411d-a322-9ecb80236c13 33 fields · synced May 31, 2026