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HiCUT Micro saw

FDA UDI

Class II (US FDA UDI)

by adeor Medical AG

Identity

Trade Name
HiCUT Micro saw FDA UDI
Generic Name
Surgical saw blade, reciprocating, single-use FDA UDI
Model / Reference
reciprocating 30 mm FDA UDI

Identifiers

Catalog Number
VMN-R-30-S FDA UDI
Primary DI / UDI-DI
04251388941850 FDA UDI
510(k) Number
K130755 FDA UDI
FDA Product Code
HBE FDA UDI
GMDN Term
Surgical saw blade, reciprocating, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4310 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical saw blade, reciprocating, single-use

HiCUT Micro saw by adeor Medical AG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical saw blade, reciprocating, single-use.

Cleared under the same submission

K130755 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
adeor Medical AG

Sources (1)

  • FDA UDI c30a787b-3118-43e6-b39c-eb877dab99ee 34 fields · synced May 30, 2026