← Back to catalogue

SCANLAN® SURG-I-BAND® color coding

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 1001-1056

by Scanlan International Inc.

Identity

Trade Name
Scanlan® SURG-I-BAND® color coding FDA UDI
Generic Name
Surgical instrument track identification tape FDA UDI
Device Name
SCANLAN® SURG-I-BAND® color coding EUDAMED
Scanlan® SURG-I-BAND® color coding - Designs on Spool, "ETO", Green, 1 spool, 1/4" width FDA UDI
Model / Reference
1001-1056 EUDAMEDFDA UDI
Description
Scanlan® SURG-I-BAND® color coding - Designs on Spool, "ETO", Green, 1 spool, 1/4" width FDA UDI

Identifiers

Catalog Number
1001-1056 FDA UDI
Primary DI / UDI-DI
00846159016109 EUDAMEDFDA UDI
Basic UDI-DI
08461590TF35LG EUDAMED
FDA Product Code
FWZ FDA UDI
EMDN Code
L80 SURGICAL INSTRUMENTS, REUSABLE - VARIOUS ACCESSORIES EUDAMED
GMDN Term
Surgical instrument track identification tape 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

Yes

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

SCANLAN® SURG-I-BAND® color coding 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 94fba7d4-1487-484c-b3b3-748cb7113f73 61 fields · synced May 29, 2026
  • FDA UDI 963bd989-9b90-4470-bea6-92a0f067ff88 35 fields · synced May 29, 2026