← Back to catalogue

BOSS Instruments

FDA UDI

Class II (US FDA UDI)

by Boss Instruments, Ltd.

Identity

Trade Name
BOSS Instruments FDA UDI
Generic Name
Surgical retractor/retraction system blade, reusable FDA UDI
Device Name
MIS Tubular Retractor, Titanium, 20mm x 8cm FDA UDI
Model / Reference
73-3070T FDA UDI
Description
MIS Tubular Retractor, Titanium, 20mm x 8cm FDA UDI

Identifiers

Catalog Number
73-3070T FDA UDI
Primary DI / UDI-DI
00888515186613 FDA UDI
FDA Product Code
GZT FDA UDI
GMDN Term
Surgical retractor/retraction system blade, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4800 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

No

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 retractor/retraction system blade, reusable

A comprehensive MIS Tubular Retractor, Titanium, 20mm x 8cm, designed for surgeons to assist with resections in neurosurgical procedures. This device features a distal component that provides precise control and separation of tissues during surgical operations.

Similar devices

Also classified as Surgical retractor/retraction system blade, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Boss Instruments, Ltd.

Sources (1)

  • FDA UDI 003622c0-c4fc-46fc-b0dc-a38a2c10f79d 35 fields · synced Jul 30, 2026