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CrocClampTM Non-Reopening Clamp

EUDAMEDFDA UDI

Class I (EU MDR)

Ref A100111

by ITL Asia Pacific Sdn. Bhd.

Identity

Trade Name
CrocClampTM Non-Reopening Clamp EUDAMED
CrocClamp™ (Non-Reopening Clamp) FDA UDI
Generic Name
Medical tubing clip/clamp, permanent FDA UDI
Device Name
CrocClamp EUDAMED
CrocClamp™ (Non-Reopening Clamp) is a device that permanently and completely occludes the tubing fluid path. FDA UDI
Model / Reference
A100111 EUDAMEDFDA UDI
Description
CrocClamp™ (Non-Reopening Clamp) is a device that permanently and completely occludes the tubing fluid path. FDA UDI

Identifiers

Catalog Number
A100111 FDA UDI
Primary DI / UDI-DI
19555240400960 EUDAMEDFDA UDI
Basic UDI-DI
955524040CCNSET EUDAMED
FDA Product Code
KSD FDA UDI
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED
GMDN Term
Medical tubing clip/clamp, permanent FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
864.9750 FDA UDI
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

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

Category: Device sterilization/disinfection container, reusable

CrocClampTM Non-Reopening Clamp by Itl Asia Pacific Sdn. Bhd. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
MY-MF-000001570
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED 8ffe904a-656b-4336-8eb6-5139e1f2ec3c 61 fields · synced Jul 9, 2026
  • FDA UDI 02ab0659-e442-412a-bf6f-031fa94fdbe4 36 fields · synced May 30, 2026