← Back to catalogue

SyringePro

FDA UDI

Class I (US FDA UDI)

by Slanted Adaptor Llc

Identity

Trade Name
SyringePro FDA UDI
Generic Name
Syringe-loaded medication/vaccine injector, manual, professional FDA UDI
Device Name
10-12 mL Standard Syringe Size, Non-sterile, Single-Use, syringe adaptor. Single patient visit use. Count 20. Syringe accessory for comfort and ergonomic support FDA UDI
Model / Reference
10mLNSSU FDA UDI
Description
10-12 mL Standard Syringe Size, Non-sterile, Single-Use, syringe adaptor. Single patient visit use. Count 20. Syringe accessory for comfort and ergonomic support FDA UDI

Identifiers

Catalog Number
10mLNSSU FDA UDI
Primary DI / UDI-DI
00860003864708 FDA UDI
FDA Product Code
IQG FDA UDI
GMDN Term
Syringe-loaded medication/vaccine injector, manual, professional FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5050 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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Syringe-loaded medication/vaccine injector, manual, professional

SyringePro by Slanted Adaptor Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Syringe-loaded medication/vaccine injector, manual, professional.

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
Slanted Adaptor Llc

Sources (1)

  • FDA UDI 901f6dd6-6146-4560-ade7-1aae9c11d820 36 fields · synced May 30, 2026