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SCANLAN® Needle Holders

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 3003-185

by Scanlan International Inc

Identity

Trade Name
SCANLAN® Needle Holders FDA UDI
SCANLAN® MicroSurgical Instruments FDA UDI
Generic Name
Suturing needle holder, reusable FDA UDI
Neurosurgical probe FDA UDI
Device Name
SCANLAN® Jacobson Micro Probe EUDAMED
Jacobson Micro Needle Holder Round Handle FDA UDI
Jacobson Micro Probe FDA UDI
Model / Reference
3003-185 EUDAMEDFDA UDI
3784-14 FDA UDI
Description
Jacobson Micro Needle Holder Round Handle FDA UDI
Jacobson Micro Probe FDA UDI

Identifiers

Catalog Number
3003-185 FDA UDI
3784-14 FDA UDI
Primary DI / UDI-DI
00846159020014 EUDAMEDFDA UDI
00846159002898 FDA UDI
Basic UDI-DI
B-00846159020014 EUDAMED
FDA Product Code
FHQ FDA UDI
GZX FDA UDI
EMDN Code
L031102 EXPLORATION PROBES, REUSABLE EUDAMED
GMDN Term
Suturing needle holder, reusable FDA UDI
Neurosurgical probe FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
876.4730 FDA UDI
882.4525 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: Suturing needle holder, reusable

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

Similar devices

Also classified as Suturing needle holder, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDD

United States Pending data

FDA UDI

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Manufacturer

Sources (3)

  • FDA UDI 30bb5fec-4c52-44f9-80f9-98ad7a16ac51 35 fields · synced Jun 18, 2026
  • FDA UDI 396385b0-257e-4ca7-afad-8472bd6b9db4 35 fields · synced May 30, 2026
  • EUDAMED f4119349-93f7-4a43-868e-17e8c5f32728 61 fields · synced Jun 18, 2026