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Syntec End Cap

FDA UDI

Class II (US FDA UDI)

by Syntec Scientific Corp.

Identity

Trade Name
Syntec End Cap FDA UDI
Generic Name
Bone nail end-cap, non-sterile FDA UDI
Device Name
Syntec End Cap φ13 x L5mm FDA UDI
Model / Reference
S880060-5 FDA UDI
Description
Syntec End Cap φ13 x L5mm FDA UDI

Identifiers

Primary DI / UDI-DI
04719873533497 FDA UDI
FDA Product Code
HWC FDA UDI
GMDN Term
Bone nail end-cap, non-sterile FDA UDI

Classification

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

Clinical & Handling

Sterile

No

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Bone nail end-cap, non-sterile

Syntec End Cap by Syntec Scientific Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone nail end-cap, non-sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Syntec Scientific Corp.

Sources (1)

  • FDA UDI c8016574-4db1-45d1-a41a-4b1561b8bd91 33 fields · synced Jun 1, 2026