← Back to catalogue

DynaNail Hybrid

FDA UDI

Class II (US FDA UDI)

by Medshape, Inc.

Identity

Trade Name
DynaNail Hybrid FDA UDI
Generic Name
Arthrodesis intramedullary nail, non-distracting FDA UDI
Device Name
DynaNail Hybrid, 7mm x 140mm FDA UDI
Model / Reference
2601-00-7140 FDA UDI
Description
DynaNail Hybrid, 7mm x 140mm FDA UDI

Identifiers

Primary DI / UDI-DI
M97026010071400 FDA UDI
510(k) Number
K203381 FDA UDI
FDA Product Code
HWC FDA UDI
JDS FDA UDI
GMDN Term
Arthrodesis intramedullary nail, non-distracting FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 FDA UDI
888.3030 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Arthrodesis intramedullary nail, non-distracting

DynaNail Hybrid by Medshape, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Arthrodesis intramedullary nail, non-distracting.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Medshape, Inc.

Sources (1)

  • FDA UDI 8b5d9763-1297-4e82-a031-042e1567d038 34 fields · synced Jun 6, 2026