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Stieber

FDA UDI

Class I (US FDA UDI)

by Automated Medical Products Corp.

Identity

Trade Name
Stieber FDA UDI
Generic Name
Surgical retraction system, reusable FDA UDI
Device Name
Stieber Small Platform Right FDA UDI
Model / Reference
Stieber Small Platform Right FDA UDI
Description
Stieber Small Platform Right FDA UDI

Identifiers

Catalog Number
SBSPFR FDA UDI
Primary DI / UDI-DI
00850023646309 FDA UDI
FDA Product Code
GAD FDA UDI
GMDN Term
Surgical retraction system, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical retraction system, reusable

Stieber by Automated Medical Products Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical retraction system, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7860ec56-c85a-48ea-a85a-719e59217939 34 fields · synced May 30, 2026