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VersaLink Torque Limiter

FDA UDI

Class II (US FDA UDI)

by Premia Spine Ltd

Identity

Trade Name
VersaLink Torque Limiter FDA UDI
Generic Name
Surgical instrument torque limiter FDA UDI
Model / Reference
87206 FDA UDI

Identifiers

Primary DI / UDI-DI
07290115932645 FDA UDI
510(k) Number
K232719 FDA UDI
FDA Product Code
NKB FDA UDI
GMDN Term
Surgical instrument torque limiter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
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 instrument torque limiter

VersaLink Torque Limiter by Premia Spine Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical instrument torque limiter.

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 72051c52-7776-4edf-951c-1974b7031f5d 33 fields · synced May 29, 2026