← Back to catalogue

Tamper Evident Cap with ENFit

FDA UDI

Class II (US FDA UDI)

by International Medical Industries Inc.

Identity

Trade Name
Tamper Evident Cap with ENFit FDA UDI
Generic Name
ENFit-formatted protective cap FDA UDI
Device Name
Tamper Evident Cap for Use With ENFit® Syringes (ETEC) FDA UDI
Model / Reference
57-220-100 FDA UDI
Description
Tamper Evident Cap for Use With ENFit® Syringes (ETEC) FDA UDI

Identifiers

Catalog Number
57-220-100 FDA UDI
Primary DI / UDI-DI
B212572201001 FDA UDI
510(k) Number
K170672 FDA UDI
FDA Product Code
PNR FDA UDI
GMDN Term
ENFit-formatted protective cap FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5980 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: ENFit-formatted protective cap

Tamper Evident Cap with ENFit by International Medical Industries Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as ENFit-formatted protective cap.

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

Sources (1)

  • FDA UDI b35479a8-0ec6-4754-bda4-e7144f3307bc 35 fields · synced May 30, 2026