Identity
- Trade Name
- Med-Syringe FDA UDI
- Generic Name
- General-purpose syringe, single-use FDA UDI
- Device Name
- 10cc Med-Syringe L/L Blue FDA UDI
- Model / Reference
- 382001 FDA UDI
- Description
- 10cc Med-Syringe L/L Blue FDA UDI
Identifiers
- Catalog Number
- 382001 FDA UDI
- Primary DI / UDI-DI
- 00886333209347 FDA UDI
- 510(k) Number
- K911732 FDA UDI
- FDA Product Code
- IZI FDA UDI
- GMDN Term
- General-purpose syringe, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 892.1600 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
Yes
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
No
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
Med-Syringe by Argon Medical Devices, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as General-purpose syringe, single-use.
- Merit Medical® — Merit Medical Systems, Inc. · Class II
- SOFT-JECT® — Henke-Sass, Wolf GmbH · Class II
- CARDINAL HEALTH — Cardinal Health 200, LLC · Class II
- SURGYCO — Surgyco LLC · Class I
- NAMIC — MEDLINE INDUSTRIES, INC. · Class II
- HSW HENKE-JECT® — Henke-Sass, Wolf GmbH · Class II
- BD Safety-Lok — BECTON DICKINSON AND COMPANY · Class II
- SURGYCO — Surgyco LLC · Class I
Cleared under the same submission
K911732 also covers:
- Control Syringe — Argon Medical Devices, Inc.
- Control Syringe — Argon Medical Devices, Inc.
- Control Syringe — Argon Medical Devices, Inc.
- Control Syringe — Argon Medical Devices, Inc.
- Med-Syringe — Argon Medical Devices, Inc.
- Med-Syringe — Argon Medical Devices, Inc.
- Med-Syringe — Argon Medical Devices, Inc.
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Argon Medical Devices, Inc.
Sources (1)
- FDA UDI 7657c60a-3b98-4ca0-968e-b361e60585ea 37 fields · synced Jun 9, 2026