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Julius Wirth

by J&J Instruments, LLC 166 variants

Part of a family of 16 devices: see the family page

Ref 736-007, 405-026, 706-006, 104-006, 736-006, 725-004, 501-009, 502-004, 507-001, 703-005, 736-010, 203-021, 730-004, 726-013, 728-003, 724-005, 105-005, 730-007, 203-012, 502-005, 203-001, 405-027, 203-008, 105-001, 733-002, 704-004, 725-007, 402-007, 207-001, 726-003, 728-002, 726-007, 701-001, 209-002, 726-009, 205-002, 509-001, 609-004, 103-002, 703-001, 704-003, 705-006, 732-001, 501-019, 405-013, 705-004, 501-014, 726-010, 208-002, 607-002, 735-001Model Dental Device

Julius Wirth (736-007) is a Class I device made by J&J Instruments, LLC, registered in EUDAMED on 15 Oct 2025 (Basic UDI-DI 08100367841660FR), active as of 22 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number08100367841660FR Basic UDI-DI Date15 Oct 2025RegisteredStatusActive

Official records

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference
Dental Device, 736-007, 405-026, 706-006, 104-006, 736-006, 725-004, 501-009, 502-004, 507-001, 703-005, 736-010, 203-021, 730-004, 726-013, 728-003, 724-005, 105-005, 730-007, 203-012, 502-005, 203-001, 405-027, 203-008, 105-001, 733-002, 704-004, 725-007, 402-007, 207-001, 726-003, 728-002, 726-007, 701-001, 209-002, 726-009, 205-002, 509-001, 609-004, 103-002, 703-001, 704-003, 705-006, 732-001, 501-019, 405-013, 705-004, 501-014, 726-010, 208-002, 607-002, 735-001
Primary DI / UDI-DI
00810036782807, 00810036781879, 00810036781008, 00810036783866, 00810036782791, 00810036782890, 00810036782272, 00810036782449, 00810036782555, 00810036780933, 00810036782838, 00810036780636, 00810036783545, 00810036784009, 00810036783507, 00810036783170, 00810036780049, 00810036783576, 00810036780735, 00810036782456, 00810036780605, 00810036781886, 00810036780698, 00810036780001, 00810036783446, 00810036781183, 00810036782920, 00810036782128, 00810036780360, 00810036783309, 00810036783491, 00810036783323, 00810036781053, 00810036780575, 00810036783347, 00810036780414, 00810036782586, 00810036781510, 00810036780469, 00810036780896, 00810036781176, 00810036780865, 00810036782692, 00810036782371, 00810036781749, 00810036780841, 00810036782326, 00810036783354, 00810036780544, 00810036781343, 00810036783675
Basic UDI-DI
08100367841660FR, 08100367833209F8, 08100367862468GU, 08100367831776G2, 08100367816480FP, 08100367835320FF, 08100367812726F4, 08100367835811G7, 08100367844887HC, 08100367866046GS, 08100367816197FR, 08100367844828GU, 08100367831848G2, 08100367831335EY, 08100367841876GJ, 08100367845713GH, 08100367815713FG, 08100367831849G4, 08100367835552G6, 08100367831878GB, 08100367835830GB, 08100367835812G9, 08100367831822FG, 08100367838168GN, 08100367855847HJ, 08100367837678HB, 08100367812235EC
EMDN code
Q010399, L150702, L0299, L160201, L1505, L159001, L159009, L0205, L159002, L150101, L15900699, L150201, L159003, L159012, L150302, Q01010199, L159099, L150301, Q01010299, L159019, L159013, L010499, L010103
Device class
Class I
EU registration type
Standard device
EU market of registration
Netherlands

Manufacturer details

EUDAMED SRN
US-MF-000008974
Authorised representative
Emergo Europe B.V. NL-AR-000000116

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Properties

  • Sterilise before use
  • Reusable NoEUDAMEDYesEUDAMED
Other properties (12, all answered No)