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Director Biopsy/Needle Guide/PullUp Probe Cover Kits

FDA UDI

by Protek Medical Products, Inc.

Identity

Trade Name
Director Biopsy/Needle Guide/PullUp Probe Cover Kits FDA UDI
Generic Name
Body-surface ultrasound imaging transducer cover FDA UDI
Model / Reference
7221 FDA UDI

Identifiers

Primary DI / UDI-DI
00841912103270 FDA UDI
GMDN Term
Body-surface ultrasound imaging transducer cover FDA UDI

Classification

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

Yes

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: Needle guide, single-useBody-surface ultrasound imaging transducer cover

Director Biopsy/Needle Guide/PullUp Probe Cover Kits by Protek Medical Products, Inc. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Body-surface ultrasound imaging transducer cover.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Protek Medical Products, Inc.

Sources (1)

  • FDA UDI 14f21348-0f6b-4c34-86d1-2c52da5dcc3d 33 fields · synced Jun 8, 2026