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Reducing sleeve

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref RTLS143746

by Joimax, Inc.

Identity

Trade Name
Reduction Tube for Laminoscopes  WCh 4.7 mm EUDAMED
Reducing sleeve FDA UDI
Generic Name
Spinal endoscopic-access system FDA UDI
Device Name
Reduction Tube for Laminoscopes  WCh 4.7 mm EUDAMED
Reduction Tube for Laminoscopes WCh 4.7 mm FDA UDI
Model / Reference
RTLS143746 EUDAMEDFDA UDI
Description
Reduction Tube for Laminoscopes WCh 4.7 mm FDA UDI

Identifiers

Catalog Number
RTLS143746 FDA UDI
Primary DI / UDI-DI
04250337115199 EUDAMEDFDA UDI
Basic UDI-DI
42503371ENSCRTDK EUDAMED
Direct Marketing DI
04250337115199 EUDAMED
FDA Product Code
NBH FDA UDI
EMDN Code
Z12021199 ORTHOPAEDIC ENDOSCOPY INSTRUMENTS - OTHER EUDAMED
GMDN Term
Spinal endoscopic-access system FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
888.1100 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Spinal endoscopic-access system

Reducing sleeve by Joimax, Inc. — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Spinal endoscopic-access system.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Joimax, Inc.

Sources (2)

  • FDA UDI 7acbb8dc-cfcc-463b-ae86-c3e159202b2e 36 fields · synced Jun 18, 2026
  • EUDAMED 6b4ff805-533e-42cb-a5f8-379a66fdb4e9 61 fields · synced Jun 18, 2026