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JETIP Instruments

EUDAMEDFDA UDI

Class I (EU MDR)

Ref noneModel JEX, JE1, JC4, JC3, JC9, JX2, JE2, JE4, JC1, JX1, JPP, JC2, JE3, JC12, JM3, JC10, JM2, JC13, JC16, JC15, JC11, JM1, JM4, JC14, JP6, JP2, JP8, JP7, JB2, JP3, JP9, JIHB, JIHY, JIHS, TJIHS, JIHG, TJIHY, TJIHB, TJIHGModel JC10

by B&L Biotech

Identity

Trade Name
JETIP Instruments EUDAMEDFDA UDI
Generic Name
Periodontal curette FDA UDI
Device Name
JETIP Instruments EUDAMED
Model / Reference
JEX, JE1, JC4, JC3, JC9, JX2, JE2, JE4, JC1, JX1, JPP, JC2, JE3, JC12, JM3, JC10, JM2, JC13, JC16, JC15, JC11, JM1, JM4, JC14, JP6, JP2, JP8, JP7, JB2, JP3, JP9, JIHB, JIHY, JIHS, TJIHS, JIHG, TJIHY, TJIHB, TJIHG EUDAMED
none EUDAMED
JC10 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
08800019115151 EUDAMEDFDA UDI
Basic UDI-DI
88000191JINSTL5 EUDAMED
B-08800019115151 EUDAMED
FDA Product Code
EMK FDA UDI
EMDN Code
Q0199 ODONTOLOGY DEVICES - OTHER EUDAMED
GMDN Term
Periodontal curette FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
872.4565 FDA UDI
Market of Registration
Denmark EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

JETIP Instruments by B&L Biotech — Class I — MDD, MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
B&L Biotech
EUDAMED SRN
KR-MF-000023296
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (4)

  • EUDAMED 51e806dd-643f-4d4a-ab88-f7e562394f7c 61 fields · synced Jul 13, 2026
  • EUDAMED 8d6eaaf2-32c6-4023-ba18-89078cb68381 61 fields · synced May 19, 2026
  • FDA UDI ed4a4ad2-6176-4541-90e1-03978200db87 32 fields · synced May 30, 2026
  • EUDAMED 51e806dd-643f-4d4a-ab88-f7e562394f7c-1 61 fields · synced Jun 10, 2026