Identity
- Trade Name
- SEEKER™ FDA UDI
- Generic Name
- Newborn metabolic screen/congenital disorder IVD, calibrator FDA UDI
- Device Name
- SEEKER™ Calibrant D FDA UDI
- Model / Reference
- 2131 FDA UDI
- Description
- SEEKER™ Calibrant D FDA UDI
Identifiers
- Catalog Number
- 2131 FDA UDI
- Primary DI / UDI-DI
- 00819704020159 FDA UDI
- 510(k) Number
- DEN150035 FDA UDI
- FDA Product Code
- JIX FDA UDI
- GMDN Term
- Newborn metabolic screen/congenital disorder IVD, calibrator FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 862.1150 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
No
FDA UDI
Category: Newborn metabolic screen/congenital disorder IVD, calibrator
Seeker™ by Baebies Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Newborn metabolic screen/congenital disorder IVD, calibrator.
- Baebies 6-HMU Dilution Set — BAEBIES INC. · Class I
- SEEKER™ — BAEBIES INC. · Class II
- SEEKER™ — BAEBIES INC. · Class II
- SEEKER™ — BAEBIES INC. · Class II
Cleared under the same submission
DEN150035 also covers:
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Baebies Inc.
Sources (1)
- FDA UDI 9fb97348-abb3-4f61-b34a-ef3752e26fbf 37 fields · synced Jun 1, 2026