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Fix connector power drill adaptor

FDA UDI

Class II (US FDA UDI)

by Premia Spine Ltd

Identity

Trade Name
Fix connector power drill adaptor FDA UDI
Generic Name
Surgical power tool adaptor FDA UDI
Model / Reference
87129 FDA UDI

Identifiers

Primary DI / UDI-DI
07290115934717 FDA UDI
PMA Number
P220002 FDA UDI
510(k) Number
K150380 FDA UDI
K170061 FDA UDI
K231844 FDA UDI
FDA Product Code
NBK FDA UDI
MNH FDA UDI
MNI FDA UDI
QWK FDA UDI
GMDN Term
Surgical power tool adaptor FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.1860 FDA UDI
888.3070 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical power tool adaptor

Fix connector power drill adaptor by Premia Spine Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical power tool adaptor.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Premia Spine Ltd

Sources (1)

  • FDA UDI 5f759c7e-2424-4874-9515-63cd3e5e5274 33 fields · synced May 31, 2026