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Sling, Knee, Kodel

FDA UDI

Class I (US FDA UDI)

by Mizuho Orthopedic Systems, Inc.

Identity

Trade Name
SLING, KNEE, KODEL FDA UDI
Generic Name
Knee sling FDA UDI
Model / Reference
334 FDA UDI

Identifiers

Catalog Number
334 FDA UDI
Primary DI / UDI-DI
00842430112690 FDA UDI
FDA Product Code
HSP FDA UDI
GMDN Term
Knee sling FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.5890 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

No

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

Category: Knee sling

Sling, Knee, Kodel by Mizuho Orthopedic Systems, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Knee sling.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 41e43ef0-bd06-4174-bf08-c3fc2e81e2c7 34 fields · synced Jun 9, 2026