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Syringe, 10 mL

FDA UDI

Class II (US FDA UDI)

by Front Line Medical Technologies Inc.

Identity

Trade Name
Syringe, 10 mL FDA UDI
Generic Name
General-purpose syringe, single-use FDA UDI
Device Name
The Syringe, 10 mL is a component of the COBRA-OS™ Kit and is used to inflate the COBRA-OS™ balloon. The COBRA-OS™ is intended for temporary occlusion of large vessels including patients requiring emergency control of hemorrhage. FDA UDI
Model / Reference
E01P3 FDA UDI
Description
The Syringe, 10 mL is a component of the COBRA-OS™ Kit and is used to inflate the COBRA-OS™ balloon. The COBRA-OS™ is intended for temporary occlusion of large vessels including patients requiring emergency control of hemorrhage. FDA UDI

Identifiers

Catalog Number
E01P3 FDA UDI
Primary DI / UDI-DI
10628678061023 FDA UDI
510(k) Number
K201652 FDA UDI
FDA Product Code
MJN FDA UDI
GMDN Term
General-purpose syringe, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4450 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

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

Dimensions & Sizes

Size
Total Volume — 10 Milliliter FDA UDI

Category: General-purpose syringe, single-use

Syringe, 10 mL by Front Line Medical Technologies Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5f79c941-8bc9-4df2-8653-6daf0554d605 36 fields · synced Jun 8, 2026