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SCANLAN® MicroSurgical Instruments

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 2813-04

by Scanlan International Inc

Identity

Trade Name
SCANLAN® MicroSurgical Instruments FDA UDI
SCANLAN® Needle Holders FDA UDI
Generic Name
Neurosurgical probe FDA UDI
Suturing needle holder, reusable FDA UDI
Device Name
SCANLAN® Grasping Forceps EUDAMED
SCANLAN® Heifetz Micro Needle Holder EUDAMED
Grasping Forceps FDA UDI
Heifetz Micro Needle Holder Round Hollow Handle FDA UDI
Model / Reference
2813-04 EUDAMEDFDA UDI
1001-52 FDA UDI
Description
Grasping Forceps FDA UDI
Heifetz Micro Needle Holder Round Hollow Handle FDA UDI

Identifiers

Catalog Number
1001-52 FDA UDI
2813-04 FDA UDI
Primary DI / UDI-DI
00846159025910 EUDAMEDFDA UDI
00846159018813 EUDAMEDFDA UDI
Basic UDI-DI
B-00846159025910 EUDAMED
B-00846159018813 EUDAMED
FDA Product Code
GZX FDA UDI
FHQ FDA UDI
EMDN Code
L031102 EXPLORATION PROBES, REUSABLE EUDAMED
L0205 NEEDLE HOLDERS, REUSABLE EUDAMED
GMDN Term
Neurosurgical probe FDA UDI
Suturing needle holder, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
882.4525 FDA UDI
876.4730 FDA UDI
Market of Registration
Netherlands EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

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: Neurosurgical probe

SCANLAN® MicroSurgical Instruments by Scanlan International Inc — Class I — MDD, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Neurosurgical probe.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDD

United States Pending data

FDA UDI

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Manufacturer

Sources (4)

  • FDA UDI 76c93342-4edf-4ffd-a687-01fd2b92cb0c 35 fields · synced Jul 14, 2026
  • FDA UDI e4b00f48-1700-4aec-9a57-bbf782031245 35 fields · synced May 30, 2026
  • EUDAMED 0a43aa24-9bec-4594-befc-7b4800119c16 61 fields · synced Jun 18, 2026
  • EUDAMED a6efabeb-85bd-45b9-a1a4-9d94fe54ac5a 61 fields · synced Jul 14, 2026