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Taurus

FDA UDI

Class II (US FDA UDI)

by CTL Medical Corporation

Identity

Trade Name
TAURUS FDA UDI
Generic Name
Internal spinal fixation procedure kit, single-use FDA UDI
Device Name
Tap, Double Lead, Cannulated, "Ø7.0 mm" FDA UDI
Model / Reference
059.7087 FDA UDI
Description
Tap, Double Lead, Cannulated, "Ø7.0 mm" FDA UDI

Identifiers

Primary DI / UDI-DI
00841732134669 FDA UDI
510(k) Number
K162160 FDA UDI
FDA Product Code
MNH FDA UDI
KWP FDA UDI
MNI FDA UDI
NKB FDA UDI
GMDN Term
Internal spinal fixation procedure kit, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3070 FDA UDI
888.3050 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Internal spinal fixation procedure kit, single-use

Taurus by CTL Medical Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Internal spinal fixation procedure kit, single-use.

Cleared under the same submission

K162160 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
CTL Medical Corporation

Sources (1)

  • FDA UDI 86af0c33-f7a4-409b-a06c-ffacd29807d8 35 fields · synced Jun 8, 2026