← Back to catalogue

Duo-Check Heat Sealing Sterilization Pouches

EUDAMEDFDA UDI

Class I (EU MDR)

Ref SC1015HSModel Sterilization Packaging

by Crosstex International Inc

Identity

Trade Name
Duo-Check Heat Sealing Sterilization Pouches EUDAMEDFDA UDI
Generic Name
Sterilization packaging, single-use FDA UDI
Device Name
Compatible with steam and EO sterilization. With internal and external process indicators, 10 in x 15 in FDA UDI
Model / Reference
Sterilization Packaging EUDAMED
SC1015HS EUDAMEDFDA UDI
Description
Compatible with steam and EO sterilization. With internal and external process indicators, 10 in x 15 in FDA UDI

Identifiers

Catalog Number
SC1015HS FDA UDI
Primary DI / UDI-DI
10732224109968 EUDAMEDFDA UDI
Basic UDI-DI
0732224SterilizationPckV5 EUDAMED
Unit of Use DI
00732224109961 EUDAMED
510(k) Number
K941327 FDA UDI
FDA Product Code
KCT 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
Germany 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

No

FDA UDI

Duo-Check Heat Sealing Sterilization Pouches by Crosstex International, Inc. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID

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-000009642
Authorised Representative
MDSS GmbH DE-AR-000005430

Sources (2)

  • EUDAMED 1ca250d7-da68-4e41-9792-5c5c4ea1be41 61 fields · synced Jun 17, 2026
  • FDA UDI 62895e5e-1017-4ce7-b9e1-edf9f3602b86 37 fields · synced May 29, 2026