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DePuy Synthes

FDA UDI

Class I (US FDA UDI)

by Provision

Identity

Trade Name
DePuy Synthes FDA UDI
Generic Name
Surgical saw blade, reciprocating, reprocessed FDA UDI
Model / Reference
05.003.422S FDA UDI

Identifiers

Primary DI / UDI-DI
B504OM05003422S0 FDA UDI
FDA Product Code
GFA FDA UDI
GMDN Term
Surgical saw blade, reciprocating, reprocessed FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4820 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

Yes

FDA UDI

Category: Surgical saw blade, reciprocating, reprocessed

DePuy Synthes by Provision — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical saw blade, reciprocating, reprocessed.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Provision

Sources (1)

  • FDA UDI 55b190a4-b3ec-4a9b-a205-29d4f5c5851e 33 fields · synced Jun 1, 2026