Pullup

FDA UDI

Class I (US FDA UDI)

by S.b.m

Identity

Trade Name: PULLUP FDA UDI
Generic Name: Suture cutter, reusable FDA UDI
Device Name: PULLUP® Cutting pliers, to be used with PULLUP and BT LOOP adjustable fixation devices for ACL reconstruction. FDA UDI
Model / Reference: Cutting pliers FDA UDI
Description: PULLUP® Cutting pliers, to be used with PULLUP and BT LOOP adjustable fixation devices for ACL reconstruction. FDA UDI

Identifiers

Catalog Number: PULL000219 FDA UDI
Primary DI / UDI-DI: 03760154006156 FDA UDI
FDA Product Code: HXZ FDA UDI
GMDN Term: Suture cutter, 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

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Suture cutter, reusable

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

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2.3MM DISPOSABLE MAXCUTTER — Biomet Orthopedics, Inc. · Class I
Trim Cord — T.A.G MEDICAL PRODUCTS AGRICULTURAL COOPERATIVE ASSOCIATION · Class I
MAXCUTTER SIDE LOAD DISPOSABLE — Biomet Orthopedics, Inc. · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: S.b.m

Sources (1)

FDA UDI f6c1cbf3-8cfa-449b-8720-273ae5a009d4 34 fields · synced May 30, 2026