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SlingShot

FDA UDI

Class I (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
SlingShot FDA UDI
Generic Name
Suturing unit, single-use FDA UDI
Device Name
SLINGSHOT 45 UP FDA UDI
Model / Reference
CAT02589 FDA UDI
Description
SLINGSHOT 45 UP FDA UDI

Identifiers

Catalog Number
CAT02589 FDA UDI
Primary DI / UDI-DI
07613252656609 FDA UDI
FDA Product Code
HWQ FDA UDI
GMDN Term
Suturing unit, single-use 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

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Angle — 45.0 degree FDA UDI

Category: Suturing unit, single-use

SlingShot by Stryker Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Suturing unit, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI 9fec5291-a243-4f3c-9ee3-5b5effb68f8f 36 fields · synced Jun 8, 2026