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Suture PassOR PRO™

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref RSG-14/18F

by The O R Company Pty Ltd

Identity

Trade Name
Suture PassOR PRO™ EUDAMED
Suture PassOR Pro FDA UDI
Generic Name
Wire/ligature passer, reusable FDA UDI
Device Name
Laparoscopic Access Device / Endoscopic Access Device EUDAMED
Model / Reference
RSG-14/18F EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
09349967000571 EUDAMEDFDA UDI
Basic UDI-DI
93499670FASCLSRE32864ZR EUDAMED
FDA Product Code
HCF FDA UDI
EMDN Code
H0199 SURGICAL SUTURES - OTHER EUDAMED
GMDN Term
Wire/ligature passer, reusable FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Market of Registration
France EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 32 Millimeter FDA UDI

Suture PassOR PRO™ by The O R Company Pty Ltd — Class IIa — 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

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Manufacturer

EUDAMED SRN
AU-MF-000010179
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (2)

  • EUDAMED 6121a79e-5775-463f-b2c8-720c84f04f82 61 fields · synced Jun 18, 2026
  • FDA UDI 646da51b-1652-4577-8e14-921cbae5ba17 33 fields · synced May 30, 2026