EUDAMED last updated this device on May 21, 2026

26933.0012

B-07630039100964

On the marketClass IIb

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: STORZ MEDICAL AG
UDI-DI code: 07630039100964
Reference / catalog number: 26933.0012

View device family (Basic UDI)

Role
Country
Date of registration
Address

EUDAMED last updated this device on May 21, 2026

26933.0012

B-07630039100964

On the marketClass IIb

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: STORZ MEDICAL AG
UDI-DI code: 07630039100964
Reference / catalog number: 26933.0012

View device family (Basic UDI)

Device identification

Trade name: not provided
UDI-DI code: 07630039100964
Basic UDI-DI: B-07630039100964
Reference / catalog number: 26933.0012
Issuing entity: GS1

Classification

Risk category: Class IIb
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)07630039100964

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

Z12040203DERMAL REGENERATION EQUIPMENT
Z12139001SHOCK WAVE THERAPY EQUIPMENT
Z120622MUSCLE STIMULATORS
Z12040205VACUUM MEDICATION EQUIPMENT
Z12101106NEUROLOGICAL STIMULATORS
Z12169004ERECTILE DYSFUNCTION STIMULATORS
Z12169002UROLOGICAL STIMULATORS

Critical warnings

3 warnings recorded — scroll inside the panel to see all entries.

CW273
EUDAMED did not publish a description for this code.
CW010
EUDAMED did not publish a description for this code.
CW016
EUDAMED did not publish a description for this code.

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

Certificates covering this device

No certificate specifically references this device's Basic UDI-DI.

Market distribution

Primary placement in France; available across 32 countries total.

Country	On market since	Until
FrancePrimary placement	May 30, 2018	Dec 31, 2028
Austria	May 30, 2018	Dec 31, 2028
Belgium	May 30, 2018	Dec 31, 2028
Bulgaria	May 30, 2018	Dec 31, 2028
Cyprus	May 30, 2018	Dec 31, 2028
Czechia	May 30, 2018	Dec 31, 2028
Germany	May 30, 2018	Dec 31, 2028
Denmark	May 30, 2018	Dec 31, 2028
Estonia	May 30, 2018	Dec 31, 2028
EL	May 30, 2018	Dec 31, 2028
Spain	May 30, 2018	Dec 31, 2028
Finland	May 30, 2018	Dec 31, 2028
Croatia	May 30, 2018	Dec 31, 2028
Hungary	May 30, 2018	Dec 31, 2028
Ireland	May 30, 2018	Dec 31, 2028
Iceland	May 30, 2018	Dec 31, 2028
Italy	May 30, 2018	Dec 31, 2028
Liechtenstein	May 30, 2018	Dec 31, 2028
Lithuania	May 30, 2018	Dec 31, 2028
Luxembourg	May 30, 2018	Dec 31, 2028
Latvia	May 30, 2018	Dec 31, 2028
Malta	May 30, 2018	Dec 31, 2028
Netherlands	May 30, 2018	Dec 31, 2028
Norway	May 30, 2018	Dec 31, 2028
Poland	May 30, 2018	Dec 31, 2028
Portugal	May 30, 2018	Dec 31, 2028
Romania	May 30, 2018	Dec 31, 2028
Sweden	May 30, 2018	Dec 31, 2028
Slovenia	May 30, 2018	Dec 31, 2028
Slovakia	May 30, 2018	Dec 31, 2028
Türkiye	May 30, 2018	Dec 31, 2028
XI	May 30, 2018	Dec 31, 2028

Device identification

Trade name: not provided
UDI-DI code: 07630039100964
Basic UDI-DI: B-07630039100964
Reference / catalog number: 26933.0012
Issuing entity: GS1

Classification

Risk category: Class IIb
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

Manufacturer information

Organization name: STORZ MEDICAL AG
SRN: CH-MF-000014374
Manufacturer status: Active

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)07630039100964

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

Z12040203DERMAL REGENERATION EQUIPMENT
Z12139001SHOCK WAVE THERAPY EQUIPMENT
Z120622MUSCLE STIMULATORS
Z12040205VACUUM MEDICATION EQUIPMENT
Z12101106NEUROLOGICAL STIMULATORS
Z12169004ERECTILE DYSFUNCTION STIMULATORS
Z12169002UROLOGICAL STIMULATORS

Critical warnings

3 warnings recorded — scroll inside the panel to see all entries.

CW273
EUDAMED did not publish a description for this code.
CW010
EUDAMED did not publish a description for this code.
CW016
EUDAMED did not publish a description for this code.

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

Certificates

Certificate health across this manufacturer's portfolio.

HZ 1620952-1Supplemented
Quality management systemNotified body: 0197Expiry: Jun 14, 2028

Certificates covering this device

No certificate specifically references this device's Basic UDI-DI.

Market distribution

Primary placement in France; available across 32 countries total.

Country	On market since	Until
FrancePrimary placement	May 30, 2018	Dec 31, 2028
Austria	May 30, 2018	Dec 31, 2028
Belgium	May 30, 2018	Dec 31, 2028
Bulgaria	May 30, 2018	Dec 31, 2028
Cyprus	May 30, 2018	Dec 31, 2028
Czechia	May 30, 2018	Dec 31, 2028
Germany	May 30, 2018	Dec 31, 2028
Denmark	May 30, 2018	Dec 31, 2028
Estonia	May 30, 2018	Dec 31, 2028
EL	May 30, 2018	Dec 31, 2028
Spain	May 30, 2018	Dec 31, 2028
Finland	May 30, 2018	Dec 31, 2028
Croatia	May 30, 2018	Dec 31, 2028
Hungary	May 30, 2018	Dec 31, 2028
Ireland	May 30, 2018	Dec 31, 2028
Iceland	May 30, 2018	Dec 31, 2028
Italy	May 30, 2018	Dec 31, 2028
Liechtenstein	May 30, 2018	Dec 31, 2028
Lithuania	May 30, 2018	Dec 31, 2028
Luxembourg	May 30, 2018	Dec 31, 2028
Latvia	May 30, 2018	Dec 31, 2028
Malta	May 30, 2018	Dec 31, 2028
Netherlands	May 30, 2018	Dec 31, 2028
Norway	May 30, 2018	Dec 31, 2028
Poland	May 30, 2018	Dec 31, 2028
Portugal	May 30, 2018	Dec 31, 2028
Romania	May 30, 2018	Dec 31, 2028
Sweden	May 30, 2018	Dec 31, 2028
Slovenia	May 30, 2018	Dec 31, 2028
Slovakia	May 30, 2018	Dec 31, 2028
Türkiye	May 30, 2018	Dec 31, 2028
XI	May 30, 2018	Dec 31, 2028

26933.0012

26933.0012

Device identification

Classification

Device details

UDI-PI traceability

UDI-DI DataMatrix

EMDN nomenclature code(s)

Critical warnings

Compliance flags

Safety

Substances

Regulatory

Lifecycle

Certificates covering this device

Market distribution

Related searches

Device identification

Classification

Device details

Manufacturer information

UDI-PI traceability

UDI-DI DataMatrix

EMDN nomenclature code(s)

Critical warnings

Compliance flags

Safety

Substances

Regulatory

Lifecycle

Certificates

Certificates covering this device

Related devices

Market distribution

Related searches

Manufacturer information

Certificates

Related devices