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Bojrab Dissection Needle, Angled 20°

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 999-DB4Model ENT Manual Reusable Surgical Instruments

by Grace Medical, Inc.

Identity

Trade Name
BOJRAB DISSECTION NEEDLE, ANGLED 20° 2.0MM STAINLESS STEEL EUDAMED
BOJRAB DISSECTION NEEDLE, ANGLED 20° FDA UDI
Generic Name
Open-surgery dissector FDA UDI
Device Name
BOJRAB DISSECTION NEEDLE, ANGLED 20° 2.0MM STAINLESS STEEL FDA UDI
Model / Reference
999-DB4 EUDAMEDFDA UDI
ENT Manual Reusable Surgical Instruments EUDAMED
Description
BOJRAB DISSECTION NEEDLE, ANGLED 20° 2.0MM STAINLESS STEEL FDA UDI

Identifiers

Primary DI / UDI-DI
00844505013727 EUDAMEDFDA UDI
Basic UDI-DI
08445050024LJ EUDAMED
Direct Marketing DI
00844505013727 EUDAMED
FDA Product Code
LRC FDA UDI
EMDN Code
L149011 ENT SURGERY DISSECTORS, REUSABLE EUDAMED
GMDN Term
Open-surgery dissector FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
874.4420 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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 Dissection Needle, Angled 20° by Grace Medical, Inc. — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Open-surgery dissector.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Grace Medical, Inc.

Sources (2)

  • FDA UDI 087bc21a-1db7-4fba-b948-118cf7484917 34 fields · synced Jul 27, 2026
  • EUDAMED c9f22e9e-c456-402e-9d59-20c4118cb55b 61 fields · synced Jul 27, 2026