← Back to catalogue

STERIKING® Pouches for robotic instruments

EUDAMEDFDA UDI

Class I (EU MDR)

Ref SSdV20

by Wipak Oy

Identity

Trade Name
STERIKING® Pouches for robotic instruments EUDAMED
Steriking® FDA UDI
Generic Name
Sterilization packaging, single-use FDA UDI
Device Name
STERIKING® Pouches and Rolls EUDAMED
Singe use sterilization packaging FDA UDI
Model / Reference
SSdV20 EUDAMEDFDA UDI
Description
Singe use sterilization packaging FDA UDI

Identifiers

Catalog Number
SSDV20 FDA UDI
Primary DI / UDI-DI
06438263665522 EUDAMED
06438263665515 FDA UDI
Basic UDI-DI
6438263ST14010NK EUDAMED
510(k) Number
K221016 FDA UDI
FDA Product Code
FRG FDA UDI
EMDN Code
S01010101 STERILISATION POUCHES, FLAT, PAPER/PLASTIC FILM EUDAMED
GMDN Term
Sterilization packaging, single-use FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
880.6850 FDA UDI
Market of Registration
Finland 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

STERIKING® Pouches for robotic instruments by Wipak Oy — 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

Manufacturer
Wipak Oy
EUDAMED SRN
FI-MF-000004496

Sources (2)

  • EUDAMED 7d19da1a-e720-4923-9771-bbe960027972 61 fields · synced Jul 9, 2026
  • FDA UDI ba2e3a4e-0563-45b2-b9b7-a6f19cc633a6 35 fields · synced May 30, 2026