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VaryFlex Neo Treatment Pack, VFNeo15/04 x 3, VFNeo 25/04 x 3, 31mm

FDA UDI

Class I (US FDA UDI)

by Endoperfection Limited

Identity

Trade Name
VaryFlex Neo Treatment Pack, VFNeo15/04 x 3, VFNeo 25/04 x 3, 31mm FDA UDI
Generic Name
Rotary/reciprocating endodontic file/rasp, single-use FDA UDI
Model / Reference
VFNEOTP31 FDA UDI

Identifiers

Primary DI / UDI-DI
05060940378817 FDA UDI
FDA Product Code
EKS FDA UDI
GMDN Term
Rotary/reciprocating endodontic file/rasp, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Rotary/reciprocating endodontic file/rasp, single-use

VaryFlex Neo Treatment Pack, VFNeo15/04 x 3, VFNeo 25/04 x 3, 31mm by Endoperfection Limited — Class I — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Rotary/reciprocating endodontic file/rasp, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 48b26c37-8dd7-408b-a221-c36fd53f2b3c 32 fields · synced May 30, 2026