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SureCare

FDA UDI

Class I (US FDA UDI)

by Ims, Inc.

Identity

Trade Name
SureCare FDA UDI
Generic Name
Polychloroprene examination/treatment glove, non-powdered FDA UDI
Model / Reference
Powder Free Chloroprene, X-Small FDA UDI

Identifiers

Primary DI / UDI-DI
00834515009117 FDA UDI
FDA Product Code
LZA FDA UDI
GMDN Term
Polychloroprene examination/treatment glove, non-powdered FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6250 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: Polychloroprene examination/treatment glove, non-powdered

SureCare by Ims, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polychloroprene examination/treatment glove, non-powdered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ims, Inc.

Sources (1)

  • FDA UDI 2e4743be-b8f8-4ee7-bddc-78b7691fe180 32 fields · synced Jun 8, 2026