← Back to catalogue

SCANLAN® TIP-GUARD™ instrument protectors

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 1001-209

by Scanlan International Inc.

Identity

Trade Name
Scanlan® TIP-GUARD™ instrument protectors - Clear FDA UDI
Generic Name
Surgical instrument guard, reusable FDA UDI
Device Name
SCANLAN® TIP-GUARD™ instrument protectors EUDAMED
Scanlan® TIP-GUARD™ instrument protectors - Original - Clear, 2.0 x 19.0 mm (100 pieces per package) FDA UDI
Model / Reference
1001-209 EUDAMEDFDA UDI
Description
Scanlan® TIP-GUARD™ instrument protectors - Original - Clear, 2.0 x 19.0 mm (100 pieces per package) FDA UDI

Identifiers

Catalog Number
1001-209 FDA UDI
Primary DI / UDI-DI
00846159001945 EUDAMEDFDA UDI
Basic UDI-DI
08461590TF21L5 EUDAMED
FDA Product Code
FWZ FDA UDI
EMDN Code
L80 SURGICAL INSTRUMENTS, REUSABLE - VARIOUS ACCESSORIES EUDAMED
GMDN Term
Surgical instrument guard, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
878.4950 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

No

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

SCANLAN® TIP-GUARD™ instrument protectors by Scanlan International Inc — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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

Manufacturer

EUDAMED SRN
US-MF-000010251
Authorised Representative
MedEnvoy Global BV NL-AR-000024028

Sources (2)

  • EUDAMED e24b9ba4-0dae-42aa-853f-9d96b33fa817 61 fields · synced Jul 22, 2026
  • FDA UDI d8ba95e0-5a77-46ab-ad15-f5c66d6239e4 35 fields · synced May 29, 2026