← Back to catalogue

General Instrument

FDA UDI

Class I (US FDA UDI)

by Camber Spine Technologies

Identity

Trade Name
General Instrument FDA UDI
Generic Name
Surgical retractor/retraction system blade, reusable FDA UDI
Device Name
Retractor Blade Clip FDA UDI
Model / Reference
CY-100-006 FDA UDI
Description
Retractor Blade Clip FDA UDI

Identifiers

Primary DI / UDI-DI
B030CY1000060 FDA UDI
FDA Product Code
GAD FDA UDI
GMDN Term
Surgical retractor/retraction system blade, 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 retractor/retraction system blade, reusable

General Instrument by Camber Spine Technologies — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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

Sources (1)

  • FDA UDI 3735e165-4230-46c2-b936-eca17e0eb882 34 fields · synced Jun 6, 2026