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Perla ® Tl Mis

FDA UDI

Class II (US FDA UDI)

by Spineart

Identity

Trade Name
PERLA ® TL MIS FDA UDI
Generic Name
Surgical instrument handle, non-torque-limiting FDA UDI
Device Name
XTAB HEAD CLIPPER FDA UDI
Model / Reference
MPF-IN 30 00-N FDA UDI
Description
XTAB HEAD CLIPPER FDA UDI

Identifiers

Catalog Number
MPF-IN 30 00-N FDA UDI
Primary DI / UDI-DI
07640450867810 FDA UDI
FDA Product Code
KWP FDA UDI
NKB FDA UDI
GMDN Term
Surgical instrument handle, non-torque-limiting FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3050 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical instrument handle, non-torque-limiting

Perla ® Tl Mis by Spineart — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical instrument handle, non-torque-limiting.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Spineart

Sources (1)

  • FDA UDI f38d1207-553f-493e-8861-be6b212b6e69 34 fields · synced May 30, 2026