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Pullup

FDA UDI

Class I (US FDA UDI)

by S.b.m

Identity

Trade Name
PULLUP FDA UDI
Generic Name
Cannulated surgical drill bit, reusable FDA UDI
Device Name
PULLUP® Ø 4.5 mm cannulated drill bit, to be used with PULLUP and BT LOOP adjustable fixation devices for ACL reconstruction. FDA UDI
Model / Reference
Drill bit FDA UDI
Description
PULLUP® Ø 4.5 mm cannulated drill bit, to be used with PULLUP and BT LOOP adjustable fixation devices for ACL reconstruction. FDA UDI

Identifiers

Catalog Number
PULL000255 FDA UDI
Primary DI / UDI-DI
03760154006163 FDA UDI
FDA Product Code
HTW FDA UDI
GMDN Term
Cannulated surgical drill bit, 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

Yes

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

Dimensions & Sizes

Size
Outer Diameter — 4.5 Millimeter FDA UDI

Category: Cannulated surgical drill bit, reusable

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

Similar devices

Also classified as Cannulated surgical drill bit, 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 3a423f97-53be-4f20-b629-7a3f7fa4bff6 35 fields · synced Jun 1, 2026