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Bookler Table Mounted Retractor Systems

FDA UDI

Class I (US FDA UDI)

by Flexbar Machine Corp.

Identity

Trade Name
Bookler Table Mounted Retractor Systems FDA UDI
Generic Name
Surgical retraction system, reusable FDA UDI
Device Name
Bookler Ratchet Bar Attachment with Hex Fitting FDA UDI
Model / Reference
69708 FDA UDI
Description
Bookler Ratchet Bar Attachment with Hex Fitting FDA UDI

Identifiers

Catalog Number
69708 FDA UDI
Primary DI / UDI-DI
00842102106170 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

Bookler 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 4a0c6041-ced3-4eef-8344-4240a7dbd773 34 fields · synced May 30, 2026