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Themy

FDA UDI

Class II (US FDA UDI)

by M.d.l. S.r.l.

Identity

Trade Name
Themy FDA UDI
Generic Name
End-cut biopsy gun handpiece/needle FDA UDI
Device Name
DISPOSABLE AUTOMATIC DEVICE 18G X 300 mm FOR SOFT TISSUE BIOPSY, NOTCH OF 20 mm FDA UDI
Model / Reference
TY1830 FDA UDI
Description
DISPOSABLE AUTOMATIC DEVICE 18G X 300 mm FOR SOFT TISSUE BIOPSY, NOTCH OF 20 mm FDA UDI

Identifiers

Catalog Number
TY1830 FDA UDI
Primary DI / UDI-DI
08056138586772 FDA UDI
510(k) Number
K160316 FDA UDI
FDA Product Code
KNW FDA UDI
FCG FDA UDI
GMDN Term
End-cut biopsy gun handpiece/needle FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1075 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
MRI Safety
MR Unsafe FDA UDI

Category: End-cut biopsy gun handpiece/needle

Themy by M.d.l. S.r.l. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as End-cut biopsy gun handpiece/needle.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
M.d.l. S.r.l.

Sources (1)

  • FDA UDI 462129be-0fac-491f-9d94-b871c01018a2 35 fields · synced Jun 1, 2026