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Home›Sweden›CAMP SCANDINAVIA AB

CAMP SCANDINAVIA AB

Sweden · Helsingborg Skane
✓ Record-verifiedregistrations found in 7 markets

This company has registrations in United States, Brazil, Saudi Arabia, Taiwan, Australia, Israel, Russia — 7 overseas markets. The China NMPA lookup is still pending.

Registrations by market

Each market counts a different unit; figures are not directly comparable
CNChinaNMPA
n/aThis registry lists domestic registrants only
EUEuropean UnionEUDAMED
pendingnot queried
USUnited StatesFDA openFDA
7listed device types
Class I 7Class II 0Class III 0
plus 7 registration records and 0 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
2registered devices
Class I 2
this export covers Class I / II only (the cadastro route)
SASaudi ArabiaSFDA
8registered imported devices
low-risk imported devices only; a 2023 snapshot, not updated since
CACanadaMDALL
0active device licences
TWTaiwanTFDA
2valid device licences
Class I 2
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
3active ARTG entries
Class I 3
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
1registrations
RURussiaRoszdravnadzor
1active registrations
Class 1 1
Not yet connected: India CDSCO, Indonesia Kemenkes. The public search for Japan PMDA and Vietnam IMDA does not return manufacturer names, so entries cannot be linked to companies coming — where there is no data it is shown as "pending", never estimated.

How these numbers were verified

record-verified

Company-name search in every official database is a substring match and returns same-named but different companies. Each figure below is the count after re-checking every record against the manufacturer name.

United States7 registration records, 0 510(k), 0 PMA, 2 excluded
Brazil2 confirmed, 0 excluded
Saudi Arabia8 confirmed, 0 excluded
Manufacturer names merged into this page: CAMP SCANDINAVIA AB

Company information

Country
Sweden
City
Helsingborg Skane

Fields marked "pending" have not been obtained yet; that does not mean they do not exist. Risk records (litigation, penalties, operating anomalies) are kept internal and not published.

FDA listed device types

Cover, Limb 1Orthosis, Limb Brace 1Joint, Knee, External Brace 1Component, External, Limb, Ankle/Foot 1Splint, Clavicle 1Splint, Hand, And Components 1Support, Arm 1

Registration details (sample)

MarketIdentifierNameClass / date
BR81284250032Órtese Plantar de CarbonoClass I
BR81284250033Ortese de CarbonoClass I
SAME0000007454SFDAA00001KiddieGAIT—
SAME0000007454SFDAA00002KiddieROCKER—

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