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Pullup-Ligafix

FDA UDI

Class I (US FDA UDI)

by S.b.m

Identity

Trade Name
PULLUP-LIGAFIX FDA UDI
Generic Name
Arthroscopic surgical procedure kit, non-medicated, reusable FDA UDI
Device Name
Complete instrumentation set composed of reusable surgical instruments intended to be used for arthroscopic reconstruction of the ACL. FDA UDI
Model / Reference
PULLUP-LIGAFIX complete ligamentoplasty instrumentation set FDA UDI
Description
Complete instrumentation set composed of reusable surgical instruments intended to be used for arthroscopic reconstruction of the ACL. FDA UDI

Identifiers

Catalog Number
PULLIG9000 FDA UDI
Primary DI / UDI-DI
03760304680793 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Arthroscopic surgical procedure kit, non-medicated, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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

Yes

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: Arthroscopic surgical procedure kit, non-medicated, reusable

Pullup-Ligafix by S.b.m — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Arthroscopic surgical procedure kit, non-medicated, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
S.b.m

Sources (1)

  • FDA UDI b731b2ba-f4f1-4554-9664-78e6203b1bbf 34 fields · synced May 30, 2026