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Mediflex Universal Round Bar Table Mounted Retractor Systems

FDA UDI

Class I (US FDA UDI)

by Flexbar Machine Corp.

Identity

Trade Name
Mediflex Universal Round Bar Table Mounted Retractor Systems FDA UDI
Generic Name
Surgical retraction system, reusable FDA UDI
Device Name
Univ TMR Small Incision Starter Sys.1,no Blades FDA UDI
Model / Reference
69601-S FDA UDI
Description
Univ TMR Small Incision Starter Sys.1,no Blades FDA UDI

Identifiers

Primary DI / UDI-DI
00842102109751 FDA UDI
FDA Product Code
FFO FDA UDI
GMDN Term
Surgical retraction system, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.4730 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

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical retraction system, reusable

Mediflex Universal Round Bar Table Mounted Retractor Systems by Flexbar Machine 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 b6e1be13-77a1-4d4f-959f-04bd1012a0f5 33 fields · synced May 31, 2026