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Bojrab Dissector, Large, Angled 20°

FDA UDI

Class I (US FDA UDI)

by Grace Medical, Inc.

Identity

Trade Name
BOJRAB DISSECTOR, LARGE, ANGLED 20° FDA UDI
Generic Name
Open-surgery dissector FDA UDI
Device Name
BOJRAB DISSECTOR, LARGE, ANGLED 20° 2.2MM x 2.0MM, L 165MM FDA UDI
Model / Reference
999-DB1 FDA UDI
Description
BOJRAB DISSECTOR, LARGE, ANGLED 20° 2.2MM x 2.0MM, L 165MM FDA UDI

Identifiers

Primary DI / UDI-DI
00844505009645 FDA UDI
FDA Product Code
LRC FDA UDI
GMDN Term
Open-surgery dissector FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4420 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: Open-surgery dissector

Bojrab Dissector, Large, Angled 20° by Grace Medical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Open-surgery dissector.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Grace Medical, Inc.

Sources (1)

  • FDA UDI 06eb881e-7789-4c68-b5ec-d39f4aa2380d 34 fields · synced May 31, 2026