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SIS Adaptor

FDA UDI

Class I (US FDA UDI)

by Surefire Medical, Inc.

Identity

Trade Name
SIS Adaptor FDA UDI
Generic Name
Frame/rail/pole device holder FDA UDI
Device Name
Surefire Infusion System Adaptor FDA UDI
Model / Reference
STA-0001 FDA UDI
Description
Surefire Infusion System Adaptor FDA UDI

Identifiers

Primary DI / UDI-DI
00857136004170 FDA UDI
FDA Product Code
FOX FDA UDI
GMDN Term
Frame/rail/pole device holder FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6990 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Frame/rail/pole device holder

SIS Adaptor by Surefire Medical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Frame/rail/pole device holder.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 119057c2-8fc7-49e3-a63f-c70f19fc4e3f 33 fields · synced May 30, 2026